Human Genetics 1994: Vol 94 Table of Contents

9 Pages·1994·0.41 MB·English

HI
Contents of Volume 94 • 1994
Baghli L Nafa K BoBhammer J —> Dork T
Abbreviations in parenthesis refer to Baiget M Valverde D Boomsma DI Beijsterveldt CEM van
the following sections: (E) Editorial; Bajalica S —» Xie Y-G Borecki IB, McGue M, Gerrard JW,
(R) Review article; (O) Original in¬ Balcells S —> Valverde D Lebowitz MD, Rao DC: Familial re¬
vestigation; (1C) Invited commentary; Ballesta F —> Mila M semblance for immunoglobulin levels
(AIC) Answer to an invited commen¬ Baralle FE Tuteja R (O) 179
tary; (SC) Short communication; (CC) Barbierato L —> Tupler R Bprresen A-L Andersen TI
Clinical case report; (CO) Case ob¬ Barbin A, Montpellier C, Kokalj-Vokac Bos AP, Pattenier AM, Grobbee RE,
served; (RG) Rare genetic variant reg¬ N, Gibaud A, Niveleau A, Malfoy B, Lindhout D, Tibboel D, Molenaar JC:
ister; (DV) DNA variants; (L) Letter to Dutrillaux B, Bourgeois CA: New sites Etiological aspects of congenital
the editors of methylcytosine-rich DNA detected diaphragmatic hernia; results of a
on metaphase chromosomes (O) 684 case comparison study (SC) 445
Barichard F —> Hamelin R Bourgeois CA —» Barbin A
Bartnitzke S —> Beige G Bourguignon J Vogt U
Baumann RE. Henschen AH: Linkage Bradley LAD —» Sweatman AK
Adams KJ Gorski SM disequilibrium relationships among Brandt B —> Lohmann DR
Adham IM Burkhardt E four polymorphisms within the human Brodeur GM —> Kaufman BA
Aguilar-Martinez P, Romey M-C, Schved fibrinogen gene cluster (O) 165 Brook-Carter P Janssen B
J-F, Gris J-C, Demaille J, Claustres M: Bayes M ^ Valverde D Brown RH Jr —> Gregor P
Factor IX gene mutations causing Behrens F —> Grade K Bruns G —> Schwartz F
haemophilia B: comparison of SSC Beijsterveldt CEM van, Boomsma Dl: Budde U —» Schneppenheim R
screening versus systematic DNA se¬ Genetics of the human electroenceph¬ Buiting K —> Dittrich B
quencing and diagnostic applications alogram (EEG) and event-related brain Bullerdiek J —» Beige G
(O) 287 potentials (ERPs): a review (R) 319 Burfeind P, Hoyer-Fender S, Doenecke
Ahmed AR —> Gibson WT Bejaoui M —> Fathallah DM D, Hochhuth C, Engel W: Expression
Ait-Abbes H Nafa K Beldjord C —> Bienvenu T and chromosomal mapping of the gene
Aksentijevich I —> Pras E Beige G, Thode B, Rippe V, Bartnitzke S, encoding the human histone H1.1 (O)
Albrechts J —» Lijnschoten G van Bullerdiek J: A characteristic sequence 633
Alcolado J Thomas AW of trisomies starting with trisomy 7 in Burkhardt E, Adham IM, Hobohm U,
Allen RJ ^ Ng WG benign thyroid tumors (SC) 198 Murphy D, Sander C, Engel W:
Allsop J —> Danpure CJ Bello D —> Viribay M A human cDNA coding for the Leydig
Almqvist E, Andrew S, Theilmann J, Belmont JW —» Leal CA insulin-like peptide (Ley I-L) (SC) 91
Goldberg P, Zeisler J, Drugge U, Bembi B —> Tuteja R Buscaglia M —» Sirchia SM
Grandell U, Tapper-Persson M, Benabadji M —> Nafa K
Winblad B, Hayden M, Anvret M: Benitez J, Fernandez E, Garcia Ruiz P, Cacheux V, Martasek P, Fougerousse F,
Geographical distribution of haplotypes Robledo M, Ramos C, Yebenes J: Tri¬ Delfau MH, Druart L, Tachdjian G,
in Swedish families with Huntington’s nucleotide (CAG) repeat expansion in Grandchamp B: Localization of the hu¬
disease (O) 124 chromosomes of Spanish patients with man coproporphyrinogen oxidase gene
Alper CA —> Gibson WT Huntington’s disea.se (SC) 563 to chromosome band 3q 12 (SC) 557
Anastasiadou V —> Hara Y Bentley D —> Lovering RC Cacurri S, Deidda G, Piazzo N, Novelletto
Andersen TI. Heimdal KR, Skrede M, Berg K —> Andersen Tl A, La Cesa I, Servidei S, Galluzzi G,
Tveit K, Berg K, Bprresen A-L: Oestro¬ Berger R —» Le Coniat M Wijmenga C, Frants RR, Felicetti L;
gen receptor (ESR) polymorphisms and Berger R Rootwelt H Chromosome 4q35 haplotypes and
breast cancer susceptibility (O) 665 Bergmann F Schneppenheim R DNA rearrangements segregating in
Andre MT Moreau-Aubry A Bernard O Labrune P affected subjects of 19 Italian families
Andreo B —> Pellestor F Bhavsar D Zheng H with facioscapulohumeral musculatur
Andrew S —> Almqvist E Bidichandani SI, Lanyon WG, Connor JM: dystrophy (FSHD) (O) 367
Angelini C —* Galvagni F Characterisation of a 5-bp deletion in Cai W —» Filosa S
Antich J Reig C exon 4 of the factor Vlll gene: concor¬ Camaschella C Totaro A
Anvret M Almqvist E dance with slipped-mispairing at DNA Cameron DP —> Teh BT
Arabien L —> Munier FL replication (SC) 447 Cantu JM —> Leal CA
Arends JW —» Lijnschoten G van Bienvenu T, Hubert D, Fonknechten N, Cao A —> Filosa S
Argarana CE —» Kleiman FE Dusser D, Kaplan JC, Beldjord C: Un¬ Cao A —> Tuteja R
Ariga T, Sakiyama Y, Matsumoto S: Two expected inactivation of acceptor con¬ Caprani M —> Gravholt CH
novel point mutations in the cytochrome sensus splice sequence by a -3 C to T Carballo M Reig C
b 558 heavy chain gene, detected in two transition in intron 2 of the CFTR gene Carbonell P Mila M
Japanese patients with X-linked chronic (O) 65 Castellvf-Bel S —» Mila M
granulomatous disease (SC) 441 Birch PH —> Gorski SM Chakraborty R —» Deka R
Arrang J-M —^ Le Coniat M Birdsey GM —» Danpure CJ Chan SP ^ Teh BT
Ashley T: Mammalian meiotic recombina¬ Bisceglia L Gasparini P Chang M-S ^ Ko Y-L
tion; a reexamination (R) 587 Blakemore AIF —> Clay FE Charlieu J-P Pellestor F
Aspillaga M —» Rios J Blankenagel A —> Drechsler M Chauveau D Plassart E
Assum G —> Hoffmeyer S Bleeker-Wagemakers EM —> Oostra R-J Chen J-J ^ Ko Y-L
Attie T —> Edery P Blennow E Xie Y-G Chen S-A ^ Ko Y-L
Audrezet MP —» Mercier B Bock D —> Schneppenheim R Chen S-H —> Thompson AR
Aupetit-Faisant B —» Clot F Bolhuis PA —> Oostra R-J Chen S-H, Zhang M, Wang N-S, Scott
Avendano I Rios J Bombieri C —> Mercier B CR; Gene frequencies of alcohol de-
Ayuso C —> Reig C Bonner WM —» Ivanova VS hydrogenasei (ADH^) and aldehyde
IV
dehydrogenase, (ALDH,) in five Chi¬ Dean M —> Pras E Druart L Cacheux V
nese minorities (SC) 571 De Andreis C —» Sirchia SM Drugge U —> Almqvist E
Cheng EY, Cartier SM: A fluorescent in De Boulle K —> Vits L Drysdale J —> Zheng H
situ hybridization analysis of X chromo¬ Debus N —> Greger V Duff GWClay FE
some pairing in early human female De Croo S Deka R Dumanski JP Xie Y-G
meiosis (O) 389 Deelen W —> Janssen B Dusser D —> Bienvenu T
Chevret E. Rousseaux S, Monteil M, Defer N —> Haber N Dutrillaux B —» Barbin A
Cozzi J, Pelletier R. Mollard J, Sele B: Deidda G Cacurri S Dziadek V —> Dork T
Male meiotic segregation of gonosomes De Jonghe P —» Nelis E
analysed by two colour FISH in human Deka R, De Croo S, Jin L, McGarvey ST, Edery P, Attie T, Mulligan LM, Pelet A,
interphase spermatozoa (SC) 701 Rothhammer F, Ferrell RE, Chakraborty Eng C, Ponder BAJ, Munnich A,
Chiang C-E ^ Ko Y-L R: Population Genetic Characteristics Lyonnet S: A novel polymorphism in
Chodirker BN —> Gorski SM of the D1S80 locus in seven human the coding sequence of the human RET
Chui DHK ^ Waye JS populations (O) 252 proto-oncogene (DV) 579
Claustres M Aguilar-Martinez P Delattre O —> Moreau-Aubry A Eisenman R Schwartz F
Clay FE. Cork MJ, Tarlow JK, Blakemore Delfau MH —> Cacheux V Ejima Y ^ Kato MV
AIF, Harrington Cl, Lewis F, Duff GW; Delhanty JDA —> Coonen E Elbaz A —> Plassart E
Interleukin 1 receptor antagonist gene Dellagi K Fathallah DM Eng B —> Waye JS
polymorphism association with lichen Delvig A —> Kukharenko V Eng C —> Edery P
sclerosus (O) 407 Demaille J Aguilar-Martinez P Engel W —> Burfeind P
Cleve H Vogt U De Mattia D —> Filosa S Engel W —> Burkhardt E
Clot F, Jager M, Simon-Bouy B, Serre JL, De Paepe A —> Rose NJ Epplen JT —> RieB O
Aupetit-Faisant B. Momet E: A poly¬ Devilder MC —> Moreau-Aubry A Espahol T —> Lovering RC
morphic poly-A sequence in the 5' re¬ Diarra-Mehrpour M —> Vogt U Est M van der —> Janssen B
gion of the aldosynthase (CYPl 1B2) Digilio MC —> Gennarelli M Estivill X —» Mercier B
gene may be useful in genetic diagnosis Dittrich B, Buiting K, GroB S, Horsthemke E.stivill X —) Mila M
of 11 P-hydroxylase genes defects (DV) B: An insertion/deletion polymorphism
316 at the D15S63 locus in the critical Fathallah DM, Bejaoui M, Sly WS,
Concannon P —> Telatar M Prader-Willi syndrome region in Lakhoua R, Dellagi K; A unique muta¬
Connor JM —> Bidichandani SI 15qll-13(DV) 583 tion underlying carbonic anhydrase II
Coonen E, Harper JC. Ramaekers FCS, Doenecke D Burfeind P deficiency syndrome in patients of Arab
Delhanty JDA, Hopman AHN, Geraedts Doerfler W —> Kochanek S descent (DV) 581
JPM, Handyside AH: Presence of chro¬ Dork T, Mekus F, Schmidt K, BoBhammer Felicetti L —> Cacurri S
mosomal mosaicism in abnormal pre¬ J, Fislage R, Heuer T, Dziadek V, Neu¬ Ferec C —^ Mercier B
implantation embryos detected by fluo¬ mann T, Kalin N, Wulbrand U, Wulf B, Fernandez E —> Benitez J
rescence in situ hybridisation (O) 609 Hardt H von der, MaaB G, Tiimmler B: Ferreira R —> Viribay M
Cooper DN —» Millar DS Detection of more than 50 different Ferrell RE —> Deka R
Cooper DN —» Wacey AI CFTR mutations in a large group of Figueiredo MS, Tavella MH, Simoes BP:
Cork MJ —> Clay FE German cystic fibrosis patients (O) Large DNA inversions, deletions, and
Coutelle C —> Grade K 533 Taq\ site mutations in severe haemo¬
Coutelle C —» Jung U Dominijanni A —> Zingone A philia A (O) 473
Coutelle C; Proceed with caution - but Donis-Keller H —» Kaufman BA Filosa S, Cai W, Galanello R, Cao A,
proceed! (AlC) 28 Donnell GN Ng WG De Mattia D, Schettini F, Martini G:
Cox DW Gibson WT Donnelly JT —> Cross GS A novel single-base mutation in the
Cozzi J —> Chevret E Doria A, Warram JH, Rich SS, glucose 6-phosphate dehydrogenase
Cross GS, Donnelly JT, Sharif AL: Krolewski AS; Angiotensin 1-converting gene is associated with chronic non-
A PvmII polymorphism near exon 2 enzyme (ACE): estimation of DNA spherocytic haemolytic anaemia (SC)
of the dystrophin gene (DV) 454 haplotypes in unrelated individuals 560
Cruciani F, Sellitto D, Santolamazza P, using denaturing gradient gel blots (O) Fislage R —> Dork T
Vespertilli T, Lerone M, Spedini G, 117 Flodman P —» Munier FL
Scozzari R; An Msp\ polymorphism in Drechsler M, Meijers-Heijboer EJ, Flori E —> Jaafar H
the X-specific region proximal to the Schneider S, Schurich B, Grond- Fonknechten N Bienvenu T
pseudoautosomal boundary. A new ex¬ Ginsbach C, Tariverdian G, Kantner G, Fontaine B —> Plassart E
ample of a unique “African” marker? Blankenagel A, Kaps D, Schroeder- Fontan G —> Lovering RC
(DV) 215 Kurth T, Royer-Pokora B: Molecular Forus A, Kools PFJ, Schoenmakers
analysis of aniridia patients for deletions EFPM, Van de Ven WJM, Myklebost
D’Alessandro M —> Salvatore M involving the Wilms’ tumor gene (O) O: A long range restriction map span¬
Dalgleish R —» Rose NJ 331 ning the myxoid liposarcoma breakpoint
Dallapiccola B —» Gennarelli M Drenth JPH, Mariman ECM, Van der in the q 13-14 region of human chromo¬
Danieli GA —> Galvagni F Velde-Visser SD, Ropers H-H, Van der some 12 (O) 259
Daniels I Janssen B Meer JWM, International Hyper-IgD Fougerousse F —> Cacheux V
Danpure CJ, Birdsey GM. Rumsby G, Study Group: Location of the gene Frants RR Cacurri S
Lumb MJ, Purdue PE, Allsop J: Molec¬ causing hyperimmunoglobulinemia D Freudine M —» Kukharenko V
ular characterization and clinical use of and periodic fever syndrome differs Friedrich U —» Gravholt CH
a polymorphic tandem repeat in an in- from that for familial mediterranean Furuyama J-1 —» Takeshita T
tron of the human alanine iglyoxylate fever (O) 616
aminotransferase gene (O) 55 Dressel R, Giinther E: A pentanucleotide Gabarron J —> Mila M
Darby JK —* Vits L tandem duplication polymorphism in Gabriel-Robez O —> Jaafar H
Das BC —> Kumar A the y untranslated region of the Galanello R —> Filosa S
Dautigny A —> Nelis E HLA-linked heat-shock protein 70-2 Galanello R Tuteja R
Davalos J Viribay M (HSP70-2) gene (DV) 585 Galluzzi G —> Cacurri S
David R Teh BT Drousiotou A —» Hara Y Galteau MM —> Panserat S
Galvagni F, Saad FA, Danieli GA, Miorin Graupner I —> Grade K Hardt H von der —> Dork T
M, Vitiello L, Mostacciuolo ML, Gravel RA Kleiman FE Harper JC Coonen E
Angelini C: A study on duplications of Gravholt CH, Caprani M, Friedrich U: Harrington Cl —> Clay FE
the dystrophin gene: evidence of a geo¬ Fluorescence in situ hybridization re¬ Harris PC —> Viribay M
graphical difference in the distribution veals a break in the a-satellite DNA of Hashimoto T —» Takeshita T
of breakpoints by intron (SC) 83 chromosome 1 in a family with a bal¬ Hassold T Zaragoza MV
Garcia Ruiz P —> Benitez J anced whole-arm translocation (O) Hayden M —» Almqvist E
Garcia-Sandoval B —¥ Reig C 504 Hayward NK Teh BT
Gartler SM Cheng EY Grebe TA Mercier B Hayworth R —» Rao PN
Gasch A —> Huschenbett J Greenberg CR —> Gorski SM Hedback G, Oden A: Parathyroid Water
Gasparini P, Grifa A, Savasta S, Merlo 1, Greengard JS ^ Tsay W Clear Cell Hyperplasia, an O-allele
Bisceglia L, Totaro A, Zelante L: The Greger V, Debus N, Lohmann D, associated condition (SC) 195
motilin gene: subregional localisation, Hopping W, Passarge E, Horsthemke B: Heimdal KR —> Andersen TI
tissue expression, DNA {xjlymorphisms Frequency and parental origin of hyper- Helio T, Palotie A, Sane T, Tikkanen MJ,
and exclusion as a candidate gene for methylated RB1 alleles in retinoblas¬ Kontula K: No evidence for linkage
the HLA-associated immotile cilia syn¬ toma (O) 491 between familial hypertriglyceridemia
drome (O) 671 Gregor P, Gaston SM, Yang X, O’Regan and apolipoprotein B, apolipoprotein
Gasparini P —> Totaro A JP, Rosen DR, Tanzi RE, Patterson D, C-III or lipoprotein lipase genes (O)
Gaston SM —> Gregor P Haines JL, Horvitz HR, Uhl GR, Brown 271
Gaudin C, Homey CJ, Ishikawa Y: Mam¬ RH Jr: Genetic and physical mapping of Hellgren D, Sahlen S, Ljungqvist S,
malian adenylyl cyclase family mem¬ the GLUR5 glutamate receptor gene on Kenne K: The human RAD51/RecA
bers are randomly located on different human chromosome 21 (SC) 565 homologue gene is not a candidate gene
chromosomes (O) 527 Grifa A —> Gasparini P for Bloom’s syndrome (SC) 705
Gean E —> Reig C Grifa A —» Totaro A Henry I —> Hamelin R
Genet SA —> Lovering RC Griffin JH ^ Tsay W Henschen AH —» Baumann RE
Gennarelli M, Novelli G, Digilio MC, Grimmond S —> Teh BT Hesseling A —> Janssen B
Giannotti A, Marino B, Dallapiccola B: Grimoldi MG —» Sirchia SM Heuer T —> Dork T
Exclusion of linkage with chromosome Grinberg D —> Valverde D Hii SI Teh BT
21 in families with recurrence of non- Gris J-C Aguilar-Martinez P Hipskind RA —> Janz M
Down’s atrioventricular canal (L) 708 Grobbee RE —> Bos AP Hobohm U —» Burkhardt E
Genuardi M Salvatore M Grond-Ginsbach C —> Drechsler M Hochhuth C —> Burfeind P
Geraedts JPM —> Coonen E GroB S —> Dittrich B Hopping W —> Greger V
Geraedts JPM —> Lijnschoten G van Gruberg L Pras E Hopping W —» Lohmann DR
Gerard N —> Panserat S Grubs R —> Rao PN Hoffmeyer S, Assum G, Kaufmann D,
Gerrard JW Borecki IB Grunewald 1 —» Grade K Schwenk K, Krone W: A deletion in
Gessler M Schwartz F Gunther E —^ Dressel R the 5'-region of the neurofibromatosis
Geurts van Kessel A —> Janz M Guimaraes J Plassart E type 1 (NFl) gene (SC) 97
Giannotti A —> Gennarelli M Guttenbach M, Schakowski R, Schmid M: H0ie K —» Rootwelt H
Gibaud A Barbin A Aneuploidy and ageing: sex chromo¬ Homey CJ —> Gaudin C
Gibson WT, Walter MA, Ahmed AR, some exclusion into micronuclei (SC) Hopman AHN —> Coonen E
Alper CA, Cox DW: The immuno¬ Hopman AHN —> Lijnschoten G van
globulin heavy chain and disease asso¬ Horsthemke B Dittrich B
ciation: application to pemphigus vul¬ Haataja R, Vaisanen M-L, Li M, Ryynanen Horsthemke B Greger V
garis (O) 675 M, Leisti J: The fragile X syndrome in Horsthemke B —» Lohmann DR
Gilgenkrantz S —> Janz M Finland: demonstration of a founder Horvitz HR —» Gregor P
Girardet A —> Pellestor F effect by analysis of microsatellite Hoyer-Fender S Burfeind P
Glover G —> Mila M haplotypes (O) 479 Hubert D —> Bienvenu T
Gnasso A —> Zingone A Haber N, Stengel D, Defer N, Roeckel N, Hulten M ^ Wallis YL
Goldberg P Almqvist E Mattel M-G, Hanoune J: Chromosomal Hunt JA —> Waye JS
Gonsalves I, Gonsalves J, Perichon B, mapping of human adenylyl cyclase Huschenbett J, Gasch A, Katzer A, Speer
Osorio-Almeida L, Krishnamoorthy R, genes type III, type V and type VI (O) A: Fine mapping of human PI 3-kinase
Lavinha J: A novel mosaic Bantu/ 69 associated p85a transcripts in the YAC
Benin/Bantu P’’ haplotype found in Hadchouel M Labrune P contig surrounding the spinal muscular
several African populations (SC) 101 Hamalainen L —» Miettinen HE atrophy gene (O) 427
Gonsalves J —> Gonsalves I Haines JL —» Gregor P Husson B Mantel A
Gonzalez-Duarte R —> Valverde D Halley D —» Janssen B
Goodfellow PJ Gorski SM Hamelin R, Barichard F, Henry I, Junien lida R —> Takeshita H
Gorski SM, Adams KJ, Birch PH, C, Thomas G: Single base pair germ¬ Imai T Tanaka T
Chodirker BN, Greenberg CR, Good- line deletion in the p53 gene in a cancer International Hyper-IgD Study Group —»
fellow PJ: Linkage analysis of X-linked predisposed family (SC) 88 Drenth JPH
cleft palate and ankyloglossia in Mani¬ Hamers G —* Smeets DFCM loannou P —> Hara Y
toba Mennonite and British Columbia Han F-Y ^ Xie Y-G Irven C —> Loughlin J
Native kindreds (O) 141 Handig I —^ Vits L Isemura S Shintani M
Grade K, Grunewald 1, Graupner I, Handyside AH —> Coonen E Ishikawa Y —> Gaudin C
Behrens F, Coutelle C: Identification Haneda N Tanaka T Ishizaki K ^ Kato MV
of three novel mutations in the CFTR Hanke R ^ Wenzel K Ito S —> Suzuki K
gene using temperature-optimized non¬ Hanoune J Haber N Ivanova VS, Zimonjic D, Popescu N,
radioactive conditions for SSCP analysis Hara Y, loannou P, Drousiotou A, Bonner WM: Chromosomal localization
(O) 154 Stylianidou G, Anastasiadou V, Suzuki of the human histone H2A.X gene to
Grade K —> Jung U K: Mutation analysis of a Sandhoff 1 Iq23.2-q23.3 by fluorescence in situ
Grandchamp B —> Cacheux V disease patient in the Maronite com¬ hybridization (SC) 303
Grandell U —> Almqvist E munity in Cyprus (O) 136 Iwata M —> Suzuki K
VI
Jaafar H. Gabriel-Robez O, Vignon F, a splice site mutation in the HEXB gene Lehmann U —> Janz M
Rori E. Rumpler Y: Supernumerary and correlation between enzyme and Lehmann-Horn F -4 Plassart E
chromosomes and spermatogenesis in a DNA-based tests for heterozygote Leisti J Haataja R
human male carrier (SC) 74 detection (O) 279 Leonard C —» Mantel A
Jacobs PA —> Zaragoza MV Klinepeter K —> Rao PN Lerone M -4 Cruciani F
Jacqz-Aigrain E —> Panserat S Ko Y-L, Chen S-A, Tang TK, Lin J-L, Levinsky RJ Lovering RC
Jager M —> Clot F Chiang C-E, Chen J-J, Teng M-S, Levinsky RJ Sweatman AK
James RS —» Zaragoza MV Chang M-S, Lien W-P, Wu C-W: No Levy E —> Pras E
Janssen B, Sampson J, Est M van der, evidence for linkage of long QT syn¬ Lewis F —> Clay FE
Deelen W, Verhoef S, Daniels 1, drome and chromosome 11 pi5.5 mark¬ Li M —> Haataja R
Hesseling A, Brook-Carter P, Nellist M, ers in a Chinese family: evidence for Lichter-Konecki U, Schlotter M, Konecki
Lindhout D, SandkuijI L, Halley D: genetic heterogeneity (O) 364 DS: DNA sequence polymorphisms in
Refined localization of TSC1 by com¬ Kochanek S, Renz D, Doerfler W: Vari¬ exonic and intronic regions of the hu¬
bined analysis of 9q34 and 16pl3 data ability in allelic DNA methylation in man phenylalanine hydroxylase gene
in 14 tuberous sclerosis families (SC) spermatozoa (SC) 203 aid in the identification of alleles (SC)
437 Kokalj-Vokac N —» Barbin A 307
Janz M. Lehmann U, Olde Weghuis D, Kok-Nazaruk MM de Oostra R-J Lien W-P -4 Ko Y-L
Leeuw B de, Geurts van Kessel A, Konecki DS Lichter-Konecki U Lijnschoten G van, Albrechts J, Vallinga
Gilgenkrantz S, Hipskind RA, Nord- Kontula K —> Helio T M, Hopman AHN, Arends JW, Geraedts
heim A: Refined mapping of the human Kontula K Miettinen HE JPM: Fluorescence in situ hybridization
Ets-related gene Elk-1 to Xpl 1.2-pl 1.4, Kools PFJ -4 Forus A on paraffin-embedded abortion material
distal to the OATLl region (SC) 442 Koritala S -4 Ng WG as a means of retrospective chromosome
Jin L —> Deka R Korpela K —> Miettinen HE analysis (O) 518
John.son EH —> Ward CXJ Krawczak M Wacey AI Lilliu F -4 Tuteja R
Jung U, Umer U, Grade K. Coutelle C: Kremer RD de Kleiman FE Lin J-L ^ Ko Y-L
Acceptability of carrier screening for Krey S -4 Schneppenheim R Lindblom A —» Tannergard P
cystic fibrosis during pregnancy in a Krishnamoorthy R -4 Gonsalves I Lindblom A Zelada-Hedman M
German population (CJ) 19 Krishnamoorthy R —> Panserat S Linde R Schneppenheim R
Junien C —> Hamelin R Kristensen T Rootwelt H Lindhout D Bos AP
Jurkat-Rott K —> Plassart E Kristoffersson U —» Xie Y-G Lindhout D —> Janssen B
Krolewski AS —* Doria A Ljungqvist S Hellgren D
Kalin N ^ Dork T Krone W -4 Hoffmeyer S Lohmann D —> Greger V
Kakkar VV -4 Millar DS Kruyer H Mila M Lohmann DR, Brandt B, Hopping W,
Kakkar VV ^ Wacey AI Kukharenko V, Sheleg S, Freudine M, Passarge E, Horsthemke B: Distinct
Kalogerakou M —» Traeger-Synodinos J Pichugina E. Delvig A: Down’s syn¬ RBI gene mutations with low pene¬
Kanavakis E —» Traeger-Synodinos J drome. Edwards’ syndrome, Patau’s trance in hereditary retinoblastoma (O)
Kaneko A —» Kato MV syndrome - synthesis of glycosamino- 349
Kantner G —» Drechsler M glycans (SC) 80 Lopez I —> Mila M
Kaplan GC —> Mercier B Kumar A, Das BC, Sharma JK: Bam\\\ re¬ Loughlin J, Irven C, Sykes B: Exclusion
Kaplan JC —* Bienvenu T striction fragment length polymorphism of the cartilage link protein and the
Kaplan J-C ^ Nafa K (RFLP) at the human GST3 gene locus cartilage matrix protein genes as the
Kaps D —» Drechsler M (RG) 107 mutant loci in several heritable chondro¬
Kastner DL —¥ Pras E Kvittingen EA —> Rootwelt H dysplasias (SC) 698
Kato MV, Ishizaki K, Shimizu T, Ejima Lovering RC, Sweatman A, Genet SA,
Y, Tanooka H, Takayama J, Kaneko A, Labrune P, Myara A, Hadchouel M, Middleton-Price HR, Vetrie D,
Toguchida J, Sasaki MS: Parental origin Ronchi F, Bernard O, Trivin F, Roy Vorechovsky 1, Bentley D, Fontan G,
of germ-line and somatic mutations in Chowdhury N, Roy Chowdhury J, Espanol T, Morgan G, Levinsky RJ,
the retinoblastoma gene (O) 31 Munnich A, Odievre M: Genetic hetero- Kinnon C: Identification of deletions
Kato N —> Tanaka T geneitiy of Crigler-Najjar syndrome in the btk gene allows unambiguous
Kattamis C —» Traeger-Synodinos J type 1: A study of 14 cases (O) 693 assessment of carrier status in families
Katzer A —> Huschenbett J La Cesa I —> Cacurri S with X-linked agammaglobulinaemia
Kaufman BA. White PS. Steinbrueck T, Lakhoua R —> Fathallah DM (SC) 77
Donis-Keller H, Brodeur GM: Linkage Landrieu P —> Mantel A Lovering RC Sweatman AK
mapping of the tumor necrosis factor Lange M —> Schneppenheim R Lucas JN —> Ward (XJ
receptor 2 (TNFR2) gene to lp36.2 Lanyon WG —» Bidichandani SI Lumb MJ Danpure CJ
using the single-strand conformation Lapie P -4 Plassart E Luthman H —> Wedell A
polymorphism technique (O) 418 Largo I —> Rios J Luzzatto L —> Nafa K
Kaufman FR ^ Ng WG Larizza D —» Tupler R Lyonnet S -4 Edery P
Kaufmann D —» Hoffmeyer S Larsson C -4 Teh BT
Keighley M ^ Wallis YL Laursen B -4 Millar DS MaaB G Dork T
Kenne K Hellgren D Lavinha J -4 Gonsalves I Macdonald F -4 Wallis YL
Kessler D —» Mercier B Law HY —» Ng ISL Mackay K Rose NJ
Khalid BAK ^ Teh BT Leal CA, Belmont JW, Nachtman R, Malfoy B Barbin A
Kihira S —> Tanaka T Cantu JM, Medina C: Parental origin of Mantel A, Leonard C, Husson B, Miladi
Kinnon C —> Lovering RC the extra chromosomes in polysomy X N, Tardieu M, Landrieu P: Submicro-
Kinnon C —» Sweatman AK (O) 423 scopic deletions of 17pl3,3 in type 1
Kino I —> Takai S Lebowitz MD -4 Borecki IB Lissencephaly (SC) 95
Kino M —» Tanaka T Le Coniat M, Traiffort E, Ruat M, Arrang Mao XQ -4 Takeshita T
Kishi K —» Takeshita H J-M, Berger R: Chromosomal localiza¬ Maraschio P -4 Tupler R
Kleiman FE. Kremer RD de. Ramirez AO tion of the human histamine H,-receptor Marasco O —> Zingone A
de. Gravel RA, Argaraha CE: Sandhoff gene (SC) 186 Marigo C —> Mercier B
disease in Argentina: high frequency of Leeuw B de ^ Janz M Mariman ECM -4 Drenth JPH
Marino B —» Gennarelli M Mollard J Chevret E Nordenskjold M Xie Y-G
Martasek P —> Cacheux V Monteil M —> Chevret E Nordenskjold M —> Zelada-Hedman M
Martin J-J —> Nelis E Montpellier C Barbin A Nordheim A —> Janz M
Martin J-P —> Vogt U Moog U —> Smeets DFCM Novelletto A —> Cacurri S
Martinez I —» Valverde D Moreau-Aubry A, Andre MT, Devilder Novell! G —> Gennarelli M
Martini G —> Filosa S MC, Resche F, Delattre O, Thomas G,
Masullo C —> Salvatore M Moisan JP: Characterization of several Oden A —» Hedback G
Matsuda M —> Takai S DNA polymorphic markers in the LIF Odievre M —> Labrune P
Matsuhashi H —> Tanaka T gene region (DV) 450 Olde Weghuis D —> Janz M
Matsui K Suzuki K Moreno F —» Viribay M Olek K Schneppenheim R
Matsui M —> Tanaka T Morgan G —> Lovering RC Onat T: Post-axial hexodactily and single
Matsumoto S —> Ariga T Morgan R Thomas AW atrium: a new syndrome? (CC) 104
Matsuoka R —> Tanaka T Morimoto K —> Takeshita T Ong JBK Ng ISL
Mattei M-G Haber N Momet E —> Clot F Oostra B —> Vits L
McClure M —> Mercier B Morral N —> Mercier B Oostra R-J, Bolhuis PA, Zom-Ende I,
McGarvey ST —> Deka R Morton DG —> Wallis YL Kok-Nazaruk MM de, Bleeker-Wage-
McGue M Borecki IB Morton JEV ^ Wallis YL makers EM: Leber’s hereditary optic
McKeown CM ^ Wallis YL Mostacciuolo ML —> Galvagni F neuropathy: no significant evidence for
Medina C —> Leal CA Mulligan LM —> Edery P primary or secondary pathogenicity of
Meijers-Heijboer El Drechsler M Munier FL, Arabien L, Flodman P, Spence the 15257 mutation (O) 265
Meili E Schneppenheim R MA, Pescia G, Rutz HP, Murphree AL: O’Regan JP Gregor P
Mekus F —> Dork T Putative non-Mendelian transmission of O’Reilly M-AJ —^ Sweatman AK
Mele E —> Zingone A retinoblastoma in males: a phenotypic Orellana O —> Rios J
Melina F —> Zingone A segregation analysis of 150 pedigrees Osborne L Rickers A
Melissari E Millar DS (O) 484 Osmani N —> Nafa K
Mendez del Castillo D —> Viribay M Munnich A —» Edery P Osorio-Almeida L Gonsalves 1
Mennon J —> Teh BT Munnich A —> Labrune P
Mercier B, Raguenes O, Estivill X, Morral Mura C Panserat S Palotie A —> Helio T
N, Kaplan GC, McClure M, Grebe TA, Murphree AL —> Munier FL Panserat S, Mura C, Gerard N, Vincent-
Kessler D, Pignatti PF, Marigo C, Murphy D —> Burkhardt E Viry M, Galteau MM, Jacqz-Aigrain E,
Bombieri C, Audrezet MP, Verlingue Myara A —> Labrune P Krishnamoorthy R: DNA haplotype-
C, Ferec C: Complete detection of Myklebost O Forus A dependent differences in the amino acid
mutations in cystic fibrosis patients of sequence of debrisoquine 4-hydroxylase
Native American origin (O) 629 Nachtman R —> Leal CA (CYP2D6): evidence for two major
Merkx GFM —* Smeets DFCM Nadano D —» Takeshita H allozymes in extensive metabolisers
Merlo 1 Gasparini P Nafa K, Reghis A, Osmani N, Baghli L, (O) 401
Merles G —> Schneppenheim R Ait-Abbes H, Benabadji M, Kaplan J-C, Parameswaran V —> Teh BT
Mesquita R —> Zelada-Hedman M Vulliamy T, Luzzatto L: At least five Parian! S Sirchia SM
Meyne J —» Ward CXj polymorphic mutants account for the Passarge E Greger V
Middleton-Price HR —» Lovering RC prevalence of glucose-6-phosphate de¬ Passarge E —> Lohmann DR
Miettinen HE, Korpela K, Hamaliiinen L. hydrogenase deficiency in Algeria (O) Pattenier AM Bos AP
Kontula K: Polymorphisms of the apo- 513 Patterson D Gregor P
lipoprotein and angiotensin converting Nagai R —> Tanaka T Pelet A —> Edery P
enzyme genes in young North Karelian Naito Y —> Takai S Pellestor F, Girardet A, Andreo B,
patients with coronary heart disease Nakahara K-I —> Tanaka T Charlieu J-P: A polymorphic alpha
(SC) 189 Nakamura Y —> Tanaka T satellite sequence spiecific for human
Mila M, Kruyer H, Glover G, Sanchez A, Nakanaga M —> Takeshita H chromosome 13 detected by oligo¬
Carbonell P, Castellvi-Bel S, Volpini V, Nancarrow DJ —> Teh BT nucleotide primed in situ labelling
Rosell J, Gabarron J, Lopez 1, Villa M, Nelis E, Timmerman V, De Jonghe P, (PRINS) (O) 346
Ballesta F, Estivill X: Molecular analy¬ Vandenberghe A, Pham-Dinh D, Pelletier R Chevret E
sis of the (CGG)„ expansion in the Dautigny A, Martin J-J, Van Broeck- Peral B Viribay M
FMR-1 gene in 59 Spanish fragile X hoven C; Rapid screening of myelin Perichon B Gonsalves I
syndrome families (O) 395 genes in CMTl patients by SSCP Perrotti N —> Zingone A
Miladi N Mantel A analysis: identification of new mutations Pescia G —> Munier FL
Millar DS, Wacey Al, Ribando J, Melis¬ and polymorphisms in the Pq gene (O) Petraroli R —> Salvatore M
sari E, Laursen B, Woods P, Kakkar 653 Pettenati MJ Rao PN
VV, Cooper DN; Three novel missense Nellist M —> Janssen B Pham-Dinh D —> Nelis E
mutations in the antithrombin III (ATS) Neoptolemos JP —> Wallis YL Piazzo N —> Cacurri S
gene causing recurrent venous thrombo¬ Neumann T Dork T Pichugina E —> Kukharenko V
sis (O) 509 Neve R —> Schwartz F Pignatti PF Mercier B
Miller RL ^ Ward OG Ng ISL, Ong JBK, Tan CL, Law HY: Piovella F —» Tupler R
Minaguchi K —> Shintani M p-Thalassemia Mutations in Singapore - Plassart E, Elbaz A, Vale Santos J,
Minchella P —> Zingone A a strategy for prenatal diagnosis (O) Reboul J, Lapie P, Chauveau D, Jurkat-
Miorin M —» Galvagni F 385 Rott K, Guimaraes J, Saudubray J-M,
Missiou-Tsangaraki S —> Traeger- Ng WG, Xu Y-K, Kaufman FR, Donnell Weis.senbach J, Lehmann-Hom F,
Synodinos J GN, Wolff J, Allen RJ, Koritala S, Fontaine B: Genetic heterogeneity
Mittler U —» Schneppenheim R Reichardt JKV: Biochemical and in hypokalemic periodic paralysis
Miyakita Y —> Tanaka T molecular studies of 132 patients with (hypoPP) (SC) 551
Mizoi Y —» Suzuki K galactosemia (O) 359 Plendl H Schneppenheim R
Moisan JP —> Moreau-Aubry A Niehof JP —» Smeets DFCM Pocchiari M Salvatore M
Molenaar JC —> Bos AP Niveleau A —> Barbin A Ponder BAJ —^ Edery P
Molinari A —> Sirchia SM Nordenskjold M —> Tannergard P Popescu N Ivanova VS
VIII
Pras E, Aksentijevich I, Levy E, Gruberg Rose NJ, Mackay K, De Paepe A, Stein- Scozzari R —> Cruciani F
L, Prosen L, Dean M, Pras M, Kastner mann B, Punnett HH, Dalgleish R: Sele B —> Chevret E
DL: The gene causing familial mediter¬ Three unrelated individuals with Sellitto D —» Cruciani F
ranean fever maps to the short arm of perinatally lethal osteogenesis imper¬ Semba T —> Shintani M
chromosome 16 in Druze and Moslem fecta resulting from identical Gly502Ser Serre JL —¥ Clot F
Arab families (SC) 576 substitutions in the a2-chain of type I Servidei S Cacurri S
Pras M -4 Pras E collagen (O) 497 SesboUe R Vogt U
Prosen L —» Pras E Rosell J —> Mila M Sharif AL —> Cross GS
Pujia A —» Zingone A Rosen DR —> Gregor P Sharma JK —> Kumar A
Punnett HH —> Rose NJ Rothhammer F —> Deka R Sheleg S —> Kukharenko V
Purdue PE —* Danpure CJ Rousseaux S Chevret E Shepherd JJ —> Teh BT
Rowe PSN: Molecular biology of hypo- Sherman S —> Zaragoza MV
Quaresima B —> Zingone A phosphataemic rickets and oncogenic Shimizu A Tanaka T
osteomalacia (R) 457 Shimizu T —> Kato MV
Raguenes O —> Mercier B Roy Chowdhury J —> Labrune P Shimokawa H —> Tanaka T
Ramaekers PCS —* Coonen E Roy Chowdhury N —> Labrune P Shintani M, Minaguchi K, Isemura S,
Ramirez AO de —» Kleiman FE Royer-Pokora B —> Drechsler M Saitoh E, Sanada K, Semba T: Genetic
Ramos C —» Benitez J Ruat M ^ Le Coniat M polymorphisms of the CST2 locus
Ramos C —> Reig C Rumpler Y —> Jaafar H coding for cystatin SA (O) 45
Rao DC Borecki IB Rumsby G Danpure CJ Simeoni E —> Schneppenheim R
Rao PN, Klinepeter K, Stewart W, Rutz HP Munier FL Simoes BP —> Figueiredo MS
Hayworth R, Grubs R, Pettenati MJ: Ryynanen M —» Haataja R Simon-Bouy B —> Clot F
Molecular cytogenetic analysis of a Simoni G Sirchia SM
duplication Xp in a male: further de¬ Saad FA —> Galvagni F Sirchia SM, De Andreis C, Pariani S,
lineation of a possible sex influencing Sahlen S Hellgren D Grimoldi MG, Molinari A, Buscaglia
region on the X chromosome (O) 149 Saitoh E —» Shintani M M, Simoni G: Chromosome 14 maternal
Reboul J Plassart E Sakiyama Y —> Ariga T uniparental disomy in the euploid cell
Rees A —» Thomas AW Salvatore M, Genuardi M, Petraroli R, line of a fetus with mosaic 46,XX/
Reghis A —» Nafa K Masullo C, D’Alessandro M, Pocchiari 47,XX,+14 karyotype (O) 355
Reichardt JKV Ng WG M: Polymorphisms of the Prion Protein Skoog L —> Zelada-Hedman M
Reig C, Antich J, Gean E, Garcia-Sando- gene in Italian patients with Creutzfeldt- Skrede M Andersen TI
val B, Ramos C, Ayuso C, Carballo M: Jakob disease (O) 375 Sly WS ^ Fathallah DM
Identification of a novel rhodopsin Sampaolo P Tupler R Smeets DFCM, Moog U, Weemaes CMR,
mutation (Met-44-Thr) in a simplex Sampson J Janssen B Vaes-Peeters G, Merkx GFM, Niehof
case of retinitis pigmentosa (O) 283 Sanada K Shintani M JP, Hamers G: ICF syndrome: a new
Reiss J —» Rickers A Sanchez A —> Mila M case and review of the literature (O)
Reiss J Rininsland F Sander C —» Burkhardt E 240
Renz D —> Kochanek S Sandkuijl L —> Janssen B Soulpi K —» Traeger-Synodinos J
Resche F —> Moreau-Aubry A Sane T Helio T Spedini G —> Cruciani F
Reyniers E —» Vits L San Millan JL Viribay M Speer A —> Huschenbett J
Ribando J —> Millar DS Sano T —> Tanaka T Speer A —> Wenzel K
Rich SS —> Doria A Santolamazza P —> Cruciani F Spence MA Munier FL
Rickers A, Rininsland F, Osborne L, Sasaki MS Kato MV Stanbridge E Tannergird P
Reiss J: Skipping of multiple CFTR Sato N —* Tanaka T Steinbrueck T —> Kaufman BA
exons is not a result of single exon Saudubray J-M -4 Plassart E Steinmann B —> Rose NJ
omissions (SC) 311 Savasta S —> Gasparini P Stengel D —> Haber N
RieB O, Winkelmann B, Epplen JT: Sawazaki K —> Takeshita H Stengler B —> Wedell A
Toward the complete genomic map and Schakowski R —» Guttenbach M Stewart W —> Rao PN
molecular pathology of human chromo¬ Schettini F —> Filosa S Stylianidou G —> Hara Y
some 4 (R) 1 Schlotter M —> Lichter-Konecki U Sugimura H —> Takai S
Rininsland F, Reiss J: Microlesions and Schmid M —> Guttenbach M Suzuki K —> Hara Y
polymorphisms in the Duchenne/Becker Schmidt K —> Dork T Suzuki K, Iwata M, Ito S, Matsui K,
muscular dystrophy gene (R) 111 Schmidtke J: Proceed with much more Uchida A, Mizoi Y: Molecular basis
Rininsland F Rickers A caution (1C) 25 for subtypic differences of the “a” sub¬
Rios J, Orellana O, Aspillaga M, Schneider S Drechsler M unit of coagulation factor XIII with
Avendano 1, Largo 1, Riveros N: CFTR Schneppenheim R, Krey S, Bergmann F, description of the genesis of the sub-
mutations in Chilean cystic fibrosis Bock D, Budde U, Lange M, Linde R, types (O) 129
patients (O) 291 Mittler U, Meili E, Mertes G, Olek K, Sweatman A —> Lovering RC
Rippe V Beige G Plendl H, Simeoni E: Genetic hetero¬ Sweatman AK, Bradley LAD, Lovering
Riveros N —» Rios J geneity of severe von Willebrand dis¬ RC, O’Reilly M-AJ, Levinsky RJ,
Robledo M Benitez J ease type 111 in the German population Kinnon C: Physical mapping in the re¬
Roeckel N -> Haber N (O) 640 gion of the Bruton’s tyrosine kinase and
Roetto A —» Totaro A Schoenmakers EFPM —» Forus A a-galactosidase A gene loci in proximal
Rogan P —> 2^agoza MV Schroeder-Kurth T —* Drechsler M Xq22 (O) 624
Romey M-C —* Aguilar-Martinez P Schurich B —> Drechsler M Sweeney M —> Thomas AW
Ronchi F —» Labrune P Schved J-F —> Aguilar-Martinez P Sykes B —> Loughlin J
Rootwelt H. Kristensen T, Berger R, Hpie Schwartz F, Neve R, Eisenman R, Gessler
K, Kvittingen EA: Tyrosinemia type 1 - M, Bruns G: A WAGR region gene Tachdjian G -> Cacheux V
complex splicing defects and a missense between PAX-6 and FSHB expressed Takai S, Tanaka M, Sugimura H, Yamada
mutation in the fumarylacetoacetase in fetal brain (O) 658 K, Naito Y, Kino I, Matsuda M: Map¬
gene (O) 235 Schwenk K —> Hoffmeyer S ping of the human C3G gene coding a
Ropers H-H —» Drenth JPH Scott CR Chen S-H guanine nucleotide releasing protein for
Ras family to 9q34.3 by fluorescence in Totaro A —> Gasparini P Vogt U, Sesboiie R, Bourguignon J,
situ hybridization (SC) 549 Totaro A, Grifa A, Roetto A, Zelante L, Diarra-Mehrpour M, Martin J-P, Cleve
Takayama J —> Kato MV Camaschella C, Gasparini P: A new H: The polymorphism of the plasma
Takeshita H, Yasuda T, Nadano D, lida R, complex polymorphic repeat close to the inter-a-trypsin inhibitor (ITl) and its
Nakanaga M, Tenjo E, Sawazaki K, HLA-A and HLA-E loci (DV) 578 relationship to the heavy chain H1 sub¬
Kishi K: Genetically polymorphic a-L- Traeger-Synodinos J, Kanavakis E, unit gene (ITIHl) at 3p211-212 (O)
fucosidase (FUCAl) isozymes detected Kalogerakou M, Soulpi K, Missiou- 39
in blood plasma (O) 224 Tsangaraki S, Kattamis C: Preliminary Volpini V —> Mila M
Takeshita T, Morimoto K, Mao XQ, mutation analysis in the phenylanaline Volz A —> Zheng H
Hashimoto T, Furuyama J-I: Characteri¬ hydroxylase gene in Greek PKU and Vorechovsky I —> Lovering RC
zation of the three genotypes of low HPA patients (SC) 573 Vulliamy T —» Nafa K
aldehyde dehydrogenase in a Japanese Traiffort E —» Le Coniat M
population (O) 217 Trivin F Labrune P Wacey AI, Krawczak M, Kakkar VV,
Tan CL Ng ISL Tsay W, Greengard JS, Griffin JH: Cooper DN: Determinants of the factor
Tan TT -> Teh BT Exonic polymorphisms in the protein C IX mutational spectrum in haemophilia
Tanaka M Takai S gene: interethnic comparison between B: an analysis of missense mutations
Tanaka T, Nakahara K-I, Kato N, Imai T, Caucasians and Asians (O) 177 using a multi-domain molecular model
Yamazaki T, Tomita H, Shimokawa H, Tiimmler B Dork T of the activated protein (O) 594
Matsuhashi H, Sato N, Matsui M, Tupler R, Barbierato L, Larizza D, Wacey AI -4 Millar DS
Kihira S, Shimizu A, Sano T, Haneda Sampaolo P, Piovella F, Maraschio P: Wallis YL, Macdonald F, Hulten M,
N, Kino M, Miyakita Y, Matsuoka R, Balanced autosomal translocations and Morton JEV, McKeown CM,
Nagai R, Yazaki Y, Nakamura Y: ovarian dysgenesis (O) 171 Neoptolemos JP, Keighley M, Morton
Genetic linkage analyses of Romano- Tuteja N Tuteja R DG: Genotype-phenotype correlation
Ward syndrome (RWS) in 13 Japanese Tuteja R, Tuteja N, Lilliu F, Bembi B, between position of constitutional APC
families (O) 380 Galanello R, Cao A, Baralle FE: gene mutation and CHRPE expression
Tang TK ^ Ko Y-L Y418C: a novel mutation in exon 9 in familial adenomatous polyjxjsis (O)
Tannergard P, Zabarovsky E, Stanbridge of the glucocerebrosidase gene of a 543
E, Nordenskjold M, Lindblom A: Sub¬ patient with Gaucher disease creates a Walter MA —> Gibson WT
localization of a locus at 3p21.3-23 new Sg/1 site (DV) 314 Walters MK ^ Teh BT
predisposing to hereditary nonpolyposis Tveit K -4 Andersen T1 Wang N-S ^ Chen S-H
colon cancer (SC) 210 Ward CJ —> Viribay M
Tanooka H —> Kato MV Uchida A —> Suzuki K Ward OG, Miller RL, Johnson EH, Lucas
Tanzi RE Gregor P Uhl GR Gregor P JN, Meyne J: Identification of trisomy
Tapper-Persson M Almqvist E Umer U Jung U in Macaca fascicularis by fluorescence
Tardieu M —> Mantel A in situ hybridization with a human chro¬
Tariverdian G —> Drechsler M Vaisiinen M-L —> Haataja R mosome 13 DNA library (O) 247
Tarlow JK Clay FE Vaes-Peeters G —> Smeets DFCM Warram JH —> Doria A
Tavella MH —> Figueiredo MS Vale Santos J -4 Plassart E Waye JS, Eng B, Hunt JA, Chui DHK:
Teh BT, Hii SI, David R, Parameswaran Valle C ^ Viribay M Filipino ^-thalassemia due to a large
V, Grimmond S, Walters MK, Tan TT, Vallinga M -4 Lijnschoten G van deletion: identification of the deletion
Nancarrow DJ, Chan SP, Mennon J, Valverde D, Bayes M, Martinez 1, Grinberg endpoints and polymerase chain reaction
Larsson C, Zaini A, Khalid BAK, D, Vilageliu L, Balcells S, Gonzalez- (PCR)-based diagnosis (O) 530
Shepherd JJ, Cameron DP, Hayward Duarte R, Baiget M: Genetic fine local¬ Wedell A, Stengler B, Luthman H:
NK: Multiple endocrine neoplasia type 1 ization of the arrestin (S-antigen) gene Characterization of mutations on the
(MENl) in two Asian families (O) 4 cM distal from D2S172 (SC) 193 rare duplicated C4/CYP21 haplotype in
468 Van Broeckhoven C —> Nelis E steroid 21 -hydroxylase deficiency (O)
Telatar M, Concannon P, Tolun A: Vandenberghe A -4 Nelis E 50
Dinucleotide repeat polymorphism at Van der Meer JWM —> Drenth JPH Weemaes CMR —> Smeets DFCM
1 lq23 (DV) 109 Van der Velde-Visser SD —> Drenth JPH Weissenbach J Plassart E
Teng M-S -» Ko Y-L Van de Ven WJM Forus A Wenzel K, Hanke R, Speer A: Poly¬
Tenjo E —> Takeshita H Verhoef S —> Janssen B morphism in the human E-.selectin
Theilmann J —> Almqvist E Verlingue C Mercier B gene detected by PCR-SSCP (DV)
Thode B —> Beige G Vespertilli T —> Cruciani F 452
Thomas AW, Morgan R, Sweeney M, Vetrie D —> Lovering RC White PS —» Kaufman BA
Rees A, Alcolado J: The detection of Vignon F —> Jaafar H Wijmenga C —> Cacurri S
mitochondrial DNA mutations using Vilageliu L —> Valverde D Willems PJ ^ Vits L
single stranded conformation poly¬ Villa M Mila M Winblad B —> Almqvist E
morphism (SSCP) analysis and hetero¬ Vincent-Viry M —> Panserat S Winkelmann B -4 RieB O
duplex analysis (O) 621 Viribay M, Ferreira R, Peral B, Bello D, Wolff J -4 Ng WG
Thomas G Hamelin R Ward CJ, Davalos J, Valle C, Harris Woods P -4 Millar DS
Thomas G Moreau-Aubry A PC, Mendez del Castillo D, Moreno F, Wu C-W ^ Ko Y-L
Thompson AR, Chen S-H; Germ line San Millan JL: Genetic analysis of Wulbrand U —4 Dork T
origins of de novo mutations in hemo¬ Cuban autosomal dominant polycystic Wulf B ^ Dork T
philia B families (SC) 299 kidney , disease kindreds using RFLPs
Tiano MT —^ Zingone A and microsatellite polymorphisms linked Xie Y-G, Han F-Y, Bajalica S, Blennow
Tibboel D —> Bos AP to the PKDl locus (O) 432 E, Kristoffersson U, Dumanski JP,
Tikkanen MJ —> Helio T Vitiello L —> Galvagni F Nordenskjold M: Identification, char¬
Timmerman V —> Nelis E Vits L, De Boulle K, Reyniers E, Handig 1, acterisation and clinical applications
Toguchida J —> Kato MV Darby JK, Oostra B, Willems PJ: Ap¬ of cosmids from the telomeric and
Tolun A Telatar M parent regression of the CGG repeat in centromeric regions of the long arm
Tomita H —» Tanaka T FMRl to an allele of normal size (O) of chromosome 22 (O) 339
Torroella M —» Zelada-Hedman M 523 Xu Y-K ^ Ng WG
X
Yamada K Takai S Zelada-Hedman M, Torroella M, Mesquita Zingone A, Dominijanni A, Mele E,
Yamazaki T —» Tanaka T R, Nordenskjold M, Skoog L, Lindblom Marasco O, Melina F, Minchella P,
Yang X —> Gregor P A: Loss of heterozygosity studies in tu¬ Quaresima B, Tiano MT, Gnasso A,
Yasuda T Takeshita H mors from families with breast-ovarian Pujia A, Perrotti N: Deletion poly¬
Yazaki Y —> Tanaka T cancer syndrome (O) 231 morphism in the gene for angiotensin
Yebenes J —» Benitez J Zelante L —> Gasparini P converting enzyme is associated with
Zelante L —> Totaro A elevated fasting blood glucose levels
Zabarovsky E —» Tannerg&rd P Zhang M —> Chen S-H (SC) 207
Zaini A —¥ Teh BT Zheng H, Bhavsar D, Volz A, Ziegler A, Zom-Ende 1 —> Oostra R-J
Zaragoza MV, Jacobs PA, James RS, Drysdale J: Exclusion of ferritins and
Rogan P, Sherman S, Hassold T: iron-responsive element (IRE)-binding
Nondisjunction of human acrocentric proteins as candidates for the hemo¬ Announcements 110, 318, 456
chromosomes: studies of 432 trisomic chromatosis gene (O) 159
fetuses and liveboms (O) 411 Ziegler A —> Zheng H
Zeisler J Almqvist E Zimonjic D —» Ivanova VS Indexed in Current Contents