7 Med Genet 1999;36:945-955 VOLUME 36: AUTHOR INDEX > Aalfs CM see Bijlsma EK et a Ballesta F Soler Aalto A-M< see Jarvinen O et al Ballhausen WG Aaltonen LA se — RW et al Balmer D e Loukola Ae Bankier A ankier A e Wang Z-] ¢ avariravan Asien, L-M see °Cc hen RW « Basber JCK Abada-Bendid M see Didierjean 10 et al e Gibbon Abbs SJ see Smith TA er al Barfoot R Abdulrazzaq YM see Amiri ak I et al Barone V C ng of the RYRI gene and Abe K see Mizushima Keet al ide itification of two novel mutations in Italian malignant Abidi F see Villard L hyperthermia { Abu- Amnere KK s Abu- Amero SN et al Barton L see P reece MA ela Bartsch O 75Se e con ations and gastric carcinoma in Abu-Amero SN see Preece MA et a Mulvihill syndrome tter, 175 Abu-Amero SN e a/. An analysis of common isodisomic regions in Bastrop R ta five mUPD 16 probands, 204 Baumbach L 1 AcheamponJgW see Jeffery S et ai Beales PL riteria for improved diagnosis of Bardet-Biedl Adams C see Waldron-Lynch F et syndrome: results of a population survey, 437 Adinolfi M see Pert! B et al Beardsall K la Neta Affara NA see Sargent CA et al Beatty B Ker Aguiar MJB see Vercesi AML Beck J El-Shanti Ajlouni K see El-Shanti H er ai Beck M< see Bung Akar N see Is onia anos G et al Beemer FA Boltshauser | Akarsu N see Zguricas J et a/ Belaich S Portnoi M-]I Al-Awadi SA see Tayel SM ¢ Belal S Didierjean O Algar EM ez al. COKNIC expression in Beckwith-Wiedemann Bellows AB syndrome patients with allele imbalance, 524 Belougne J Al-Gazali L see Amirlak I er a/ see V ill ard I Al-Gazali LI ez a/. Absent pituitary gland and hypoplasia of the Beltran- Valero de rey abe D Mutational analysis of the cerebellar vermis associated with partial ophthalmoplegia and HGO gene in Finnis iulkaptonuria patients, 922 postaxial polydactyly: a variant of orofaciodigital syndrome VI or Benitez J see Sanc I é a new syndrome?, 161 Benomar A see Didierjear Complex consanguinity associated with short rib-polydactyly Bentsi-Enchill E syndrome III and congenital infection-lik e syndrome: a diagnostic Bernard JP problem in dysmorphic syndromes, 461 Besley G Shim« Alho A see Beltran-Valero de Bernabé D er al Bespalova IN Ali Z see Abu-Amero SN ez al Bessant DAR see Preece MA et al Bevan S ‘the MHC region to the familial risk of Aliberti F see de Brasi D er al coeliac dise Allanson JE et al. The face of Smith-Magenis syndrome a subjective Bhattacharya SS and objective study, 394 Biarnes J Sanchez Allen-Powell DR see Wilcox SA et ai Biesecker L Al-Naggar RL see Tayel SM er al Biggs P Alpert L see Yuan ZQ et al Bignon JD Al-Salem M<« see El-Shanti H er a/ Bignon Y-] Al-Shahri A see El-Harith E-HA et a! Bijlsma EK ryptic translocation between Altuntas B see Loudianos G et al chromosomes 2qter an¢ i 8qter: further delineation of the Amiel J see Bonnet D er a/ Albright hereditary osteodystrophy- like phenotype, 604 ee Manouvrier-Hanu §S ez al Bird AC Payne AM Amiel J er a/. Epiphyseal, vertebral, and ear (EVE dysplasia: a new Biros I, = S. Spinal muscular atrophy: untangling the knot?: syndrome?, 561 Amirlak I e7 a/. A syndrome of immune complex glomerulonephritis Mishap DT e Froggatt NJ and ophthalmic abnormalities, 641 Bitoun P see David A et a Amoah-DanquahJ see Jeffery S er al Bjarnadottir K see Tulinius H Amor D et al. 46,XX/46,XY at amniocentesis in a fetus with true Black GCM see Doward W et a hermaphroditism: letter, 866 Blackwell JM Searle S and Blackwell JM Amorim A see Munar-Qués M et al Bland M< see Jeffer tal Andrassi M see Gehrig A et al Bleik J see Mégar ¢ Andreutti-Zaugg C see Yuan ZQ et a Blennow E, Sahleén S. Rescue from the effects of trisomy Andrews RM< see Chinnery PF er a/ 13q32—qter owing to skewed X inactivation in a see Chinnery PF et al der(X)t(X;13)(p21;q32) carrier: letter, 718 Andria G see de Brasi D et al Bobba A . 21-hydroxylase deficiency in Italy: a distinct Angius A see Loudianos G et al distribution pattern of CYP2/ mutations in a sample from Anthony K see Yuan ZQ et al southern Italy: /etter, 648 Antinolo G see Borrego S et al Bobrow M Smith TA et a see Sanchez B et al Bogdanow A see Shanske AL et a Aoki M see Mizushima K et al Boltshauser EJ et ai. Coexistence of Gaucher disease type 1 and Aradhya §S see Heiss NS et al Joubert syndrome: /etter, 870 ArslanE see Murgia A et al Bomford AB see Walker AP et a Arslanian A see Di Rocco M er al BonaventureJ see Lajeunie E et al Arvio M see Arvio P et al Bonduelle M see Goelen G«e t Arvio P ez al. Overgrowth of oral mucosa and facial skin, a novel Boner AL Trabetti E « feature of aspartylglucosaminuria, 398 Bonino M-C see Villard L Audrézet MP see Férec C et al Bonne G sex Ric hard P et al Austin-Ward ED, Taucher SC. Familial congenit: wdd iz _ agmatic Bonnefont J-P see Villard L et al hernia: is an imprinting mechanism involved?: letter, $78 Bonnet D et a Tricuspid atresia and conotruncal malformations in Avizienyte E see Chen RW et al five families: /etter, 349 see Wang Z-J et al Boogaerts A se Decruyenacre 4 et al Book reviews Milunsky A, editor. Genetic disorders and the fetus. Bagolan P see Digilio MC et al Diagnosis, prevention anc f treatment, 655 Bakir M< see Al-Gazali LI ez al Borck G see Wirth J et al Bakker E see van der Maarel SM et al Borrego S see Sanchez B et al Bakker L see van Slegtenhorst M et al Borrego S et al. Specific polymorphisms in the RET proto-oncogene Bakker PLG see Laan LAEM et a/ are over-represented in patients with Hirschsprung disease and Bakker R see van Slegtenhorst M et al may represent loci a phenotypic expression, 771 Bakker W see ZguricasJ et al Borrelli P see Stuppia L Author index Borrone C see Di Rocco M et al Celebi JT et a/. Phenotypic findings of Cowden syndrome and Botta A et al. Detection of an atypical 7q11.23 deletion in Williams Bannayan-Zonana syndrome in a family associated with a single syndrome patients which does not include the STX1A and germline mutation in PTEN, 360 FZD3 genes, 478 Chandler M< see Christianson AL et al Boucher CA see Sargent CA er 2! Chang-Claude J see Shugart YY er a/ Bouscarat F see Portnoi M-F et al Chapman P see Shankar A ert al Boutchnei S see Portnoi M-F ez a/ Charron P see Richard P et al Bouvier R see Faivre L er al Chen FF see Celebi JT et al Bowden DW see Hart TC et al Chen RW et al. PTEN and LKB! genes in laryngeal tumours: /etter, Bracco A see Barone V et al 943 Bradshaw JM see Cornish KM er al Chinnery PF ez a/. Clinical mitochondrial genetics: review, 425 Brady AF er ai. Clinical and molecular findings in a patient with a Mitochondrial DNA analysis: polymorphisms and pathogenicity: deletion on the long arm of chromosome 12 : /etter, 939 review, 505 Braegger CP see Bevan S et al Chitty L see Lees MM et al Brambati B see Pertl B et al Chong WKK see Hoveyda N et al Brassett C see Froggatt NJ er a/ Choo KHA see Slater HR et a/ see Verma L et al Choueiri R see Mégarbané A et al Brecevic L see Utkus A er al Chowdhury T see Reardon W et al Breedveld G see Zguricas J et al Christianson AL et a/. X linked severe mental retardation, Breen CJ et al. Applications of comparative genomic hybridisation in craniofacial dysmorphology, epilepsy, ophthalmoplegia, and constitutional chromosome studies, 511 cerebellar atrophy in a large South African kindred is localised to Breines E see Fagerheim T ez a/ Xq24-q27, 759 Bremer M< see Dork T er al Christophis P see Steinberger D ert a/ Breukel C see Kartheuser A et al Churchman M< see Wang Z-J et al Breuning MH see Brooks AS et al Cibis GW see Fitzgerald KM et a/ Briard M-L see Faivre L er al Ciccodicola A see Heiss NS et a/ Briault S see Villard L er al Claes S see Stromme P et al Brice A see Didierjean O et al Claustres M see Romey M-C et a/ see Dirr A et al Clayton-SmithJ see Slavotinek A et ai Briones P see Muro S et al Clenaghan C see Tischkowitz M et al Britton K see Reardon W et al Cloostermans T see Decruyenaere M er a Brondum-Nielsen K see Wirth J et a/ Coelho T see Munar-Queés M et al BrookJD see Hamshere MG er al Coéslier A see Manouvrier-Hanu § et al Brookfield JFY see Hamshere MG et al Coffey R see Reardon W et al Brooks AS ez a/. A consanguineous family with Hirschsprung Cole GF see Moore SJ et al disease, microcephaly, and mental retardation Cole TRP see Lam WWK et al (Goldberg-Shprintzen syndrome), 485 Colleaux L see Villard L er al Brown G see Sargent CA et al Collins FS see Hacia JG and Collins FS Brox V see Fagerheim T er a! Conn CM er al. Preimplantation genetic diagnosis for couples at high Budarf ML see Kerstjens-Frederikse WS et a/ risk of Down syndrome pregnancy owing to parental Bugge M see Wirth J er al translocation or mosaicism, 45 Bunge S er al. Mucopolysaccharidosis type IIIB (Sanfilippo B): Conway G see Murray A et al identification of 18 novel a-N-acetylglucosaminidase gene Cook L et al. 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International variation in reported livebirth chromosome 18: additional evidence of autoimmunity or IDDM prevalence rates of Down syndrome, adjusted for maternal age, gene(s) on chromosome 18, 156 386 da Fonseca N see Saraiva JM et al Carrier L see Richard P et al Dagna-Bricarelli F see Di Rocco M et al Carrio A see Soler A et al Dahl H-HM see Wilcox SA et al Carroll BT ez al. Polymorphisms in PTEN in breast cancer families, Dallaire L see Farrell SA et al 94 Dallapiccola B see Botta A er al Carvalho MRS see Vercesi AML ert al see Digilio MC et al Casey E see Amor D et al Dalton P see Robinson DO et a/ Cassiman JJ see Decruyenaere M et al Daniel CP see Liling J et al Cassiman J-J see Stromme P et al Darnfors C see Wahlstrém J et al Castel T see Ruiz A et al Da-Silva EO see Leal GF and Da-Silva EO Catsman CE see Brooks AS et al David A et al. Hydrometrocolpos and polydactyly: a common Catsman-Berrevoets CE see Laan LAEM et al neonatal presentation of Bardet-Biedl and McKusick-Kaufman see Voznyi YV et al syndromes, 599 Author index Davies AF ez a/. An interstitial deletion of 6p24-p25 proximal to the see Lodder LN eta FKHL/7 locus and including AP-2a that affects anterior eye Dunham I see Gardner RJ chamber development, 708 Dunlop A see Breen CJ et al Davies § see Tischkowitz M et al Dupont C Férec ( see Wang Z-J et al Dupont J-M ez a/. Unexpected Angelman syndrome molecular defect Davis AC see Parker MJ et al in a girl displaying clinical features of Prader-Willi syndrome: Dawodu A see Al-Gazali LI et al letter, 652 Dean JCS see Moore SJ et al Durand C Sargent CA de Brasi D ez a/. Cloverleaf skull anomaly and de novo trisomy 4p Durr A Did ean O et a letter, 422 Durr A et al. H Ozyzosit y in Huntington’s disease: /etter, 172 de Cordoba SR see Beltran-Valero de Bernabé D er ai D’Urso M see Heiss NS Decruyenaere M< er ail. Psychological functioning before predictive testing for Huntington’s disease: the role of the parental disease, Earle E see S ater HR risk perception, and subjective proximity of the disease, 897 Easton D see Shugart YY et a de Die-Smulders CEM see Janssen HCJP er al Eastwood JB see Jeffery S et a Deeble GJ see Algar EM er al Eccles D see Shugart YY et 2 de Gréve J see Goelen G et al Edwards YH see Papapetrou C er a Deichmann KA ez a/. Linkage and association studies of atopy and Eeles RA Hodgson SV et al the chromosome 11q13 region, 379 Eich G see Superti-Furga A et al Deidda G see van der Maarel SM et al Elcioglu N see Beales PL et ai Deineko NL see Ivanova-Smolenskaya IA et al El Ghouzzi V see Lajeunie E et a de la Chapelle A see Loukola A er al Elhaji Y see van Orsouw NJ ez a see Lynch HT and de la Chapelle A El-Harith E-HA ez ai. Identification and clinical presentation of 8 Delaroziere JC see Moncla A et al thalassaemia n ns in the eastern region of Saudi Arabia: Delatycki MB see Amor D et al letter, 935 Delatycki MB er a/. Directly inherited partial trisomy of illis D Hodgson SV chromosome 6p identified in a father and daughter by lis I see Wang Z-] et a chromosome microdissection, 335 -Najjar M see El-Shanti H ez Delezoide A-L see Odent S et ai sawi MM < see Brady AF et a Delezoide A-L see Faivre L et al 21-Shanti H ez a/. A nonsense mutation in the retinal specific Delhanty JDA see Conn CM et al guanylate cyclase gene is the cause of Leber congenital amaurosis de los Angeles Ibanez M see Valero R et al in a large inbred kindred from Jordan: /etter, 862 Delpech M see Dupont J-M ez al Emanuel BS see Kerstjens-Frederikse WS et al Demaille J see Romey M-C et al Emmerich P see Schuffenhauer S et al Demirhan O see Coucke PJ er a/ Eng C see Borrego S et al Demyttenaere K see Decruyenaere M er al see Myers SM et al Denavit M-F see Dupont J-M ez al see van Orsouw NJ et a Dennis N see Murray A et al Esposito T see Heiss NS et a Denton MJ see Gu S-M et al Estivill X see Rabionet R and Estivill X Derry C et al. A probable case of familial Weaver syndrome see Ruiz A et al associated with neoplasia: /etter, 725 Evans DGR Douglas FS Dersarkissian H see Portnoi M-F er al see Froggatt NJ et a Dessi V see Loudianos G et al see McGaughran JM Detry R see Kartheuser A et al see Verma L et a Devilee P see Lodder LN er al see Wang Z-J et a Everett LA see Coucke PJ et a see Shugart YY et al Evers-Kiebooms G see Decruyenaere M et al Devriendt K ez a/. Triplication of distal chromosome 10q, 242 Eyre H see Callen DF de Vries BBA see Macpherson J et al de Vries BBA er a/. Dilemmas in counselling females with the fragile Faber H Kok K et al X syndrome, 167 Fagerheim T ez a/. A new gene DY X3) for dyslexia is located on Screening for the fragile X syndrome among the mentally retarded chromosome 2, 664 a clinical study, 467 Homozygosity mapping to the USH2A locus in two isolated Dhanda RK see van Orsouw NJ et a/ populations, 144 Didierjean O et a/. Linkage disequilibrium at the SCA2 locus, 415 Faivre L ez al. A new lethal syndrome of exomphalos, short limbs, Dietrich NL see Coucke PJ et al and macrogonadism, 131 di Gilio MC see Stuppia L er al Falth-Magnusson K see Bevan S et al Digilio MC see Botta A et al Fang Y-Y see Callen DF et al Digilio MC ez al. Microdeletion 22q11 and oesophageal atresia, 137 Faravelli F ez a/. Unusual clustering of brain tumours in a family Dijkhuizen T see Kok K ez al with NF! and variable expression of cutaneous features, 893 di Maio S see Bobba A et al Faria E see Saraiva JM et al Di Martino A see Barone V er al Farrell SA et a/. Club foot, an adverse outcome of early di Micco P see de Brasi D er al amniocentesis: disruption or deformation?, 843 Dinis A see Saraiva JM et al Faure C see Férec C et al Di Rocco M< et ai. Ataxia, ocular telangiectasia, chromosome FeingoldJ see Diirr A et al instability, and Langerhans cell histiocytosis in a patient with an Feingold M. Costello syndrome and rhabdomyosarcoma: letter, 582 unknown breakage syndrome, 159 Férec C et al. Mutations in the cationic trypsinogen gene and Dobbie Z, Miller H. Germline mutations in the B-catenin gene are evidence for genetic heterogeneity in hereditary pancreatitis, 228 not associated with the FAP phenotype without an APC Ferak V see Plasilova M et al mutation: etter, 573 Ferakova E see PlaSilova M et al Dodé C see Diirr A et al Ferguson A see Bevan S et a Dom R see Decruyenaere M et al see Wang Z-J et al Donatien Y see Richard P et a/ Fergusson W see Slavotinek A et al Donnai D see Lam WWK et al Fermont L see Bonnet D er a/ see McGaughran JM et al Fernandez JL see Mosquera A et al see Slavotinek A et al Fichera M< see Villard L et a/ Dooley JS see Walker AP et al Finnell RH see Shaw GM et al Dork T et a/. BRCAI expression is not affected by the intronic 12 bp Fiorente P see Gentile M et al duplication: letter, 262 Firatli E see Hart TC et al Douglas FS ez al. 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High frequency of BRCA1/2 germline mutations in brothers with the fragile X syndrome: different CGG repeats and 42 Belgian families with a small number of symptomatic different mental capacities, 253 subjects, 304 Henderson K see Kerstjens-Frederikse WS et ai Goessling A see Myers SM et al Hennekam RCM see Bijlsma EK er al Goldgar D see Shugart YY er a/ see van den Berg H and Hennekam RCM Goldman A see Padoa C et al Heredero-Baute L see Zguricas J et al Gomes C see Saraiva JM er al Heuertz §S see Heiss NS et al Gonzalez-Duarte R see Valero R et al Heus H see Zguricas J et al GoodshipJ see Shankar A et al Heutink P see Zguricas J et al Gordon PH see Yuan ZQ et al Hewitt JE see van der Maarel SM et al Gosalvez J see Mosquera A et al Hii S see Teh BT et al Goyanes VJ see Mosquera A et al Hinson RM< see Frizzley JK er al Gravel RA see Shaw GM et al Hirschhorn R, Huie ML. 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The critical region of overlap defining the AZFa Smith ACM Allanson JE er male infertility interval of proximal Yq contains three transcribed Smith PJ see Algar EM sequences, 670 Smith RJH see ¢ oucke PJ er Sarret E see Valero R et al Sarri C see Dacou-Voutetakis C er a/ see van Camp Sartorelli MR see Loudianos G er al Smith S Saut N see Sargent CA et al Smith TA Savage MO see Brady AF et al mosaicisn a point mutation in a Duchenne muscular Savarirayan R, Bankier A. Simpson-Golabi-Behmel syndrome and dystropl amily, 313 attention deficit hyperactivity disorder in two brothers: /etter, 574 Snead MP, Yates JRW. Clinical and molecular genetics of Stickler Schaap C see Janssen HCJP et al syndrome: review, 353 Schaefer HE see Walter K et al Séderling I see Jarvinen O Schalling M see Teh BT et al Soler A et a/. Trisomy/tetrasomy 21 mosaicism in CVS: Scheffer H see Hordijk R er a/ interpretation of cytogenetic discrepancies between placental and Scheidl T see Kerstjens-Frederikse WS er a/ fetal chromosome complements, 333 Schiffmann D see Papp T er al Solomon E Hodgson SV et a Schinzel A see Guttenbach M er al Sorokina I see Utkus A see Utkus A et al Sorrentino V see Barone V et Schlenther S see Deichmann KA er al Souied E see Rozet J-M et a Schmeits J see Verma L et al Sparholt SH see Deichmann KA et al Schmid M see Guttenbach M et al Spitz L see Papapetrou C et al Schmidt R see Shanske AL er al Spranger J see Superti-Furga A et al Schmidtke J see El-Harith E-HA et al Springbett S see Suthers G et a Schoenmakers E see Devriendt K et a/ Srikumari CR see Gu S-M et al Schofield PN see Lam WWK er al Stagni ML see Genuardi M et « Scholl T ez a/. Biochemical and genetic characterisation shows that Stallings RL 3reen CJ et al the BRCA1 IVS20 insertion is a polymorphism: /etter, 571 Stanhope R see Price SM et al Schrander JJP see Moog U et al Stanier P see Abu-Amero SN Schrander-Stumpel CTRM see Kok K et al see Preece MA et al see Moog U et al Starke B see Deichmann KA et a/ Schuffenhauer § er a/. De novo deletion (14)(q11.2q13) including Stastna §S see Kozak L et a PAX9: clinical and molecular findings, 233 Steglich C see Bunge S et a Schwartz C see Villard L er al Steinberger D ez ai. Mutation of FGFR2 (cys278phe) in Schwartz CE see Christianson AL er al craniolacunia and pansynostosis: /etter, 499 Schwartz K see Richard P er al Steinlein C see Guttenbach M et al Schwartz M see Orstavik KH ez al Steinmann B see Superti-Furga A er al Schwinger E see Bartsch O et al Stenhammer L see Bevan S et al Seal S see Shugart YY ez al Stephan MJ see Frizzley JK et ai Searle S, Blackwell JM. Evidence for a functional repeat Stevanin G see Didierjean O et al polymorphism in the promoter of the human NRAMP!1 gene Stevenson RE see Christianson AL et ai that correlates with autoimmune versus infectious disease Stine OC see Margolis RL et a/ susceptibility, 295 Stoilov I see Plasilova M et al Seaver L see Villard L er al Stolte-Dijkstra I see Hordijk R et al Sebastio G see de Brasi D et al Stone EM< see El-Shanti H et a/ Sequeiros J see Munar-Qués M er al Stoppa-Lyonnet D see Shugart YY et al Sertedaki A see Dacou-Voutetakis C er a/ Strachan T see Lako M et al Seruca R see Caldas C et al Strain L see Moore SJ et al see Munar-Ques M et al Stratton M see Shugart YY et ai Setianingsih I see Pramoonjago P er a/ Shaffer LG see Slavotinek A et al see Teh BT et al see Wu Y-Q et al Stromme P ez ai. X linked mental retardation and infantile spasms Shanahan F see Waldron-Lynch F et a/ in a family: new clinical data and linkage to Xp11.4-Xp22.11, Shankar A ez ai. Genetic counselling: do we recognise and meet the 374 consultands’ agenda?: letter, 580 Stuhrmann M<« see Dérk T et ai Shanske AL et a/. Simultaneous occurrence of two supernumerary see El-Harith E-HA et a/ autosomal ring chromosomes r(1) and r(16) in twins, 625 Stuppia L et a/. Loss of the SHOX gene associated with Leri-Weill Shapira SK see Slavotinek A et al dyschondrosteosis in a 45,X male, 711 Shashi V ez a/. Genetic heterogeneity of gingival fibromatosis on Sturniolo GC see Loudianos G er al chromosome 2p, 683 Summers AM < see Farrell SA et al Shather W see Al-Gazali LI er al Sundet K see Stromme P et a/ Shaw GM < ez a/. Infant methionine synthase variants and risk for Super M see McGaughran JM et al spina bifida: /etter, 86 Superti-Furga A ez a/. Recessively inherited multiple epiphyseal Sheffield VC see El-Shanti H er al dysplasia with normal stature, club foot, and double layered Sherr M see Margolis RL er al patella caused by a DTDST mutation, 621 Shield JPH see Gardner RJ et al Susman M see Amor D et al see Hoveyda N et al Suthers G er a/. Skewed sex ratios in familial holoprosencephaly and Shimozawa N ez al. Defective PEX gene products correlate with the in people with isolated single maxillary central incisor, 924 protein import, biochemical abnormalities, and phenotypic Suzuki Y see Shimozawa N et al heterogeneity in peroxisome biogenesis disorders, 779 Swallow DM < ez ai. Ulcerative colitis is not associated with differences Shizuka M see Mizushima K er a/ in MUC2 mucin allele length: /etter, 859 Shkolny DL see Frizzley JK et al Sweeney E ez a/. Smith-Magenis syndrome and tetralogy of Fallot: Shoji M see Mizushima K et al letter, 501 Shugart YY ez a/. Linkage analysis of 56 multiplex families excludes Szarras-Czapnik M see Kusz K et al the Cowden disease gene PTEN as a major contributor to Sztriha L see Al-Gazali LI er al familial breast cancer: /etter, 720 see Al-Gazali LI et al Author index Taillemite J-L see Portnoi M-F er al see van Slegtenhorst M et al Tan SY see Gibbons B er al van den Ouweland AMW see de Vries BBA er a/ Taneda H see Miyoshi O er al see Laan LAEM et al Taucher SC see Austin-Ward ED and Taucher SC van der Maarel S see Wirth J et a Taufani RA see Pramoonjago P et al van der Maarel SM< ez a/. A new dosage test for subtelomeric 4;10 Tawn EJ see Liling J et al translocations improves conventional diagnosis of Tayel SM er al. Familial pericentric inversion of chromosome | facioscapulohumeral muscular dystrophy (FSHD), 823 (p36.3q23) and Bardet-Biedl syndrome: /erter, 418 van der Meer CA see Lodder LN et ai Teare D see McGaughran JM et al van der Meyden CH see Christianson Al see Shugart YY et al van der Veen AY see Kok K et a Teebi AS see Kennedy SJ ez a/ van der Wielen MJR see van der Maarel SM er Tegazzin V see Barone V et al Vandevijver N see Janssen HCJP er a Teh BT et al. Familial testicular cancer: lack of evidence for van Diggelen OP see Bunge S et a trinucleotide repeat expansions and association with PKD1 in see Voznyi YV et al one family: /etter, 348 van Essen AJ see Kerstjens-Frederikse WS Tempelaars A see van Slegtenhorst M er al van Hauwe P see Coucke PJ et a Temple IK see Derry C et al van Ooij A see Moog U et a see Gardner RJ et al van Orsouw NJ et a/. A highly accurate, k ww cost test for BRCA1 Terriou P see Sargent CA er al mutations, 747 Teshima I see Kerstjens-Frederikse WS et al van Rensburg PL see Christianson Al Teugels E see Goelen G et al van Rijn M see de Vries BBA et ai Theron FW see Christianson AL et al van Royen-KerkhofA see Boltshauser EJ et a Thompson JN see Li P et a/ van Slegtenhorst M< ez a/. Mutational spectrum of the TSC1 gene in Thompson MH see Hoveyda N et al a cohort of 225 tuberous sclerosis complex patients: no evidence Thomson APJ et a/. Autosomal dominant optic atrophy with for genotype-phenotype correlation, 285 unilateral facial palsy: a new hereditary condition?, 251 Varady E see Al-Gazali LI et al Tibben A see de Vries BBA et al Vasseur C see Dupont J-M er a see de Vries BBA et al vd Smagt JJV see Brooks AS er a see Lodder LN et al Vekemans M< see Faivre L et a Tiranti V er a/. Leigh syndrome transmitted by uniparental disomy of Veleba A see Callen DF et al chromosome 9: letter, 927 Venkat-Raman K see Derry C et al Tischkowitz M et a/. Amelogenesis imperfecta, sensorineural hearing Vercesi AML ez a/. Prevalence of Prader-Willi and Angelman loss, and Beau’s lines: a second case report of Heimler’s syndromes among mentally retarded boys in Brazil: /etter, 498 syndrome: /etter, 941 Verellen-Dumoulin C see Kartheuser A e7 a Todoroff K see Shaw GM et al VerhoefS see Tischkowitz M et al Tofeig M see Sweeney E et al see van Slegtenhorst M et a Tomlinson IPM see Wang Z-J et al Verloes A see David A et al Tommerup N see Wirth J et al Verma L ez ail. Mononucleotide microsatellite instability and Tonnby B see Wahlstrém J er al germline MSH6 mutation analysis in early onset colorectal Tonnessen FE see Fagerheim T et a/ cancer, 678 Torrisi L see Genuardi M et a/ Verstreken M see van Camp G et Tozzi C see Genuardi M et al VigneronJ see David A et al Trabetti E ez al. Association of a lymphotoxin « gene polymorphism Vijg J see van Orsouw NJ et a and atopy in Italian families, 323 Vilchez JJ see Garcia-Planells J et al Tranebjerg L see Fagerheim T et a/ Villard L et a/. Evaluation of a mutation screening strategy for see Fagerheim T et al sporadic cases of ATR-X syndrome, 183 Trembath R see Coucke PJ et a/ Two unrelated patients with inversions of the X chromosome and see Reardon W et al non-specific mental retardation: physical and transcriptional Trembath RC see Bijlsma EK er a/ mapping of their common breakpoint region in Xq13.1, 754 see Price SM et al Vinall LE see Swallow DM et al Trifiro M see Yuan ZQ et al Vinanzi C see Murgia A et a/ Trijsburg RW see Lodder LN et a/ Voelckel M-A see Moncla A et a! Trundley A see Sargent CA et al Vogelsang H see Caldas C et al Tryggvadottir L see Tulinius H et al Voisey J see MacMillan JC et al Tsou HC see Celebi JT et al Volpini V see Sanchez B et a Tsukamoto T see Shimozawa N et al von Deimling A see Myers SM et a Tulinius H et a/. Breast cancer incidence and familiality in Iceland von Kap-Herr C see Shashi V er a/ during 75 years from 1921 to 1995, 103 Voullaire L see Delatycki MB er al Tului L see Pert! B et al Voznyi YV et a/. A new simple enzyme assay for pre- and postnatal Turnbull DM see Chinnery PF et al diagnosis of infantile neuronal ceroid lipofuscinosis (INCL) and see Chinnery PF et al its variants, 471 Tyler-Smith C see Tzancheva M et al Vujic M see Wahlstrém J er al Tympner K-D see Bartsch O et al Tzancheva M er al. Two male patients with ring Y: definition of an Wagner A see Lodder LN et a interval in Yq contributing to Turner syndrome, 549 WahlstrémJ ez a/. Congenital variant Rett syndrome in a girl with terminal deletion of chromosome 3p, 343 Ugarte M see Muro S et al Wakeling EL see Preece MA et al Uller A see Wahlstrém J et al Waldron-Lynch F et a/. Genetic analysis of the 3' untranslated Ulrich V er al. The inheritance of migraine with aura estimated by region of the tumour necrosis factor shows a highly conserved means of structural equation modelling, 225 region in rheumatoid arthritis affected and unaffected subjects, Upadhyaya M see Faravelli F ez al 214 Utkus A er al. Duplication of segment 1p21 following paternal Walker AP er al. Atypical haemochromatosis: phenotypic spectrum insertional translocation, ins(6;1)(q25;p13.3p22.1), 73 and f,-microglobulin candidate gene analysis, 537 Uutela A see Jarvinen O ert al Walker SJ see Hart TC er al Uziel G see Tiranti V et al Walker-Smith J see Bevan S er a/ Wallace DF see Walker AP et al Vabres P see Heiss NS et al Wallis YL ez ai. Molecular analysis of the APC gene in 205 families: Valenzano MC see Gentile M et al extended genotype-phenotype correlations in FAP and evidence Valero R et a/. Molecular characterisation of partial chromosome 21 for the role of APC amino acid changes in colorectal cancer aneuploidies by fluorescent PCR, 694 predisposition, 14 Vallée L see Manouvrier-Hanu S et al Walon C see Kartheuser A et al van Camp G see Coucke PJ et al Walter K et al. Sequence analysis of the homogentisate 1,2 van Camp G er al. A gene for autosomal dominant hearing dioxygenase gene in a family affected by alkaptonuria: /etter, 645 impairment (DFNA14) maps to a region on chromosome Wanders RJA see Shimozawa N et al 4p 16.3 that does not overlap the DFNA6 locus, 532 Wang Q see van Slegtenhorst M et al Vance GH see Cook L et al Wang Z-J et a/. Germline mutations of the LKB! STK11) gene in van de Heyning PH see van Camp G er al Peutz-Jeghers patients, 365 van den Berg H, Hennekam RCM. Acute lymphoblastic leukaemia Ward B see Scholl T et al in a patient with cardiofaciocutaneous syndrome: letter, 799 Ward CM see Margolis RL er al van den Boer-van den Berg HMA see de Vries BBA et al Warenik-Szymankiewicz A see Kusz K er al van den Helm B see Hamel BCJ er ai Warne G see Amor D et al van den Ouweland A see Shugart YY et a/ Watanabe M< see Mizushima K er al

Journal of Medical Genetics 1999: Vol 36 Index

Similar Journal of Medical Genetics 1999: Vol 36 Index