Annals of Human Genetics 1999: Vol 63 Index

9 Pages·1999·2.6 MB·English

INDEX. Vol.
Abulhasan, 8S. J.. Tayel, S. M. & Al-Awadi, S. A. model using familial hy percholesterolemia and aorto
mosaic Turner syndrome: cytogenetics versus FISH, coronary calcification, 511
199 Attwood, T. K. & Parry-Smith. D. J. eds
Al-Awadi, S. A. Introduction to Bi? oinfor matics reviewed by H.M
see Abulhasan, S. J. et al. Wain. 381
Alif, N., Hess, K., Straezek. J.. Sebbar. is N'bou. A..
Nabet, P. & Dousset, B. Bandelt. H.-J.
mucopolysaccharidosis tvpe I: characterization of a see Rando, J.C. et al
common mutation that causes Hurler syndrome in Bartfay. E., Donner, A. & Klar, N
Moroccan subjects, 9 testing the equality of twin correlations with multi
Alitalo, T. nomial outcomes, 341
see Huopaniemi, L. ef al. Berchtold, S. Jones, T.. Muhl-Zurbes. P Sheer 1)
alternatively spliced isoforms. Molecular cloning, func Schuler G. & Steinkasserer A
tional characterization and genomic organization of the human dendritic cell marker CD83 maps to chro
four...of the human organic cation transporter | mosome 6p23, 181
(hROCT1/SLC22A 1), 473 Bergen, A. W.. Wang. C.-\ Tsai, J Jeffer son K Dey
Al-Zahery, N. C.. Smith, K. D Park. S.-C Tsai. S.-J & Goldman,
see Quintana-Murci, L. ef al. D
aminopeptidase n gene. Linkage disequilibrium between an Asian- Native American paternal lineage identified
intra-locus variants in the...and test of their by RPS4Y resequencing and by microsatellite haplo
association with coeliac disease. 207 typing, 63
Amorim, A. Berkovic, S. F.. Genton, P.. Hirsch, E. & Pieard, F. eds
Genetics of E pilepsies reviewed by M. Gardiner. 274
see Carvalho. F. et al.
Bijkerk, C.
angiotensin II subtype 1 (AT1) receptor gene. Character
see Meulenbelt. | et al
ization of polymorphisms in the promoter of the
Blangero. As
human, 369
see Williams, J. T.
angiotensinogen. Evidence of a major gene effect for...
Boenisch, H.
among Nigerians, 293
SEF Haver, M.
apolipoprotein B gene. Evolution of the... and coronary
Boerwinkle. E.
artery disease: a study in low and high risk Asians.
see Hallman, D. M. ef al
45
Bolognesi. 5.
apolipoprotein E (APOE) allele distribution in the world
see Giordano, M et al
Is APOE*4 a ‘thrifty’ allele? 301
Breakefield. X. O.
apolipoprotein E genotype. Influence of.. . Variation on
see Klein. C. ef al
the means, variances, and correlations of plasma
Breedveld, F.C
lipids and apolipoproteins in children, 311
see Meulenbelt, [. et al
Arinami, T., Lijima, Y., Yamakawa-Kobayashi. K..
Brega. A
Ishiguro, H., Ohtsuki, T., Yanagi, H.. Shimakura. see Quintana-Murei. L et al
Y., Ishikawa H. & Hamaguchi H.
Brett. P. M., Yiannakou, J. Y.. Morris. M-A Vaughan.
supportive evidence for contribution of the dopamine
R.. Curtis. D. & Ciclitira, P. J
D2 receptor gene to heritability of stature: linkage
common HLA alleles, rather than rare mutants, confer
and association studies, 147 susceptibility to coeliac disease 217
Arlen Price, R. British. Detailed haplotype analysis in Ashkenazi Jewish
see Li, W.-D. ef al. and non-Jewish ... dystonic patients carrying the
Arnett, D. K. GAG deletion in the DYTI gene: evidence for a
see Coon, H. et al. limited number of founder mutations. 1
Ashkenazi Jewish. Detailed haplotype analysis in... and British. New DNA markers with increased informative
non-Jewish British dystonic patients carrying the ness show diminished support for a chromosome
GAG deletion in the DYTI gene: evidence for -a oqil 13 schizophrenia susceptibility locus and ex
limited number of founder mutations, | lude linkage in two new cohorts of... and Icelandic
Asian. An... Native American paternal lineage identi families, 235
fied by RPS4Y resequencing and by microsatellite Brorholt-Petersen, J. U
haplotyping, 63 see Jensen, J. M. ef al
Asians. Evolution of the apolipoprotein B gene and Bruess, M.
coronary artery disease: a study in low and high see Haver, M
risk, 45 Bruni, N., Rajas. F.. Montano, S Chevalier-Porst, F
association studies. Supportive evidence for contribution Maire I. & Mithieux. G
of the dopamine D2 receptor gene to heritability of enzymatic characterization of four new mutations in
stature: linkage and, 147 the glucose 6 phosph itase gene W hich cause glycogen
atherosclerosis. Linking genotype to aorto-coronary ... storage disease tvpe la, 141
Index
Brynjolfsson, J. Collins, A.
Sé€E€ Kalsi, G. et al. see Gomes, I. et al.
Collins, A.
Cabrera, V. M. see Scapoli, C. et al.
see Rando, J. C. et al. conformation-sensitive gel electrophoresis. Superiority of
Campbell, L. J. denaturing high performance liquid chromatography
see Chadwick, B. P. et al. over single-stranded conformation and... for mu-
Canary Islands. Phylogeographic patterns of mtDNA tation detection in TSC2, 383
reflecting the colonization of the, 413 Coon, H., Leppert, M. F., Kronenberg, F., Province, M.
Carvalho, F., Peixoto, A., Steffensen, R., Amorim, A.. A., Myers, R.H., Arnett, D. K., Eckfeldt, J. H.,
David, L. & Sobrinho-Simoes, M. Heiss, G., Williams, R. R. & Hunt, 8. C.
MUC1 gene polymorphism does not explain the evidence for a major gene accounting for mild elevation
different incidence of gastric cancer in Portugal and in LDL cholesterol: The NHLBI Family Heart
Denmark, 187 Study, 401
Casari, G. Cooper, R.
see Giordano, M. et al. see Guo, X. et al.
CD83. The human dendritic cell marker...maps_ to Corbo, R. M. & Seacchi, R.
chromosome 6p23, 181 apolipoprotein E (APOE) allele distribution in the
Chadwick, B. P., Campbell, L. J., Jackson, C. L., Ozelius, world. Is APOE*4 a ‘thrifty’ allele? 301
L.. Slaugenhaupt, S.A., Stephenson, DA... coronary artery disease. Evolution of the apolipoprotein
Edwards, J. H., Wiest J. & Povey S. B gene and...: a study in low and high risk Asians,
report on the 1998 International Chromosome 9 Work- 45
shop, 101 Cossu, G.
Cheung, V.G. see Quintana-Murci, L. ef al.
see Grant, G. R. et al. Curtis, D.
Chevalier-Porst, F. see Brett, P. M. et al.
see Bruni, N. ef al. Curtis, D.
Chi-square. Relative efficiencies of the ... recombination see Kalsi. G. ef al.
models for gene mapping with human pedigree data,
81 Dabora. S. L.
Choy, Y.S., Dabora, S. L., Hall, F.. Ramesh, V., Niida, see Choy, Y _S. et al.
Y.. Franz. D., Kasprzyk-Obara, J., Reeve, M. P. & D’alfonso, S.
Kwiatkowski, D. J. see Giordano. M. et al.
superiority of denaturing high performance liquid David, L.
chromatography over single-stranded conformation see Carvalho, F. et al,
and conformation-sensitive gel electrophoresis for Davis. M. B.
mutation detection in TSC2, 383 see Valente. E. M. et al.
Christiansen, T.M De La Chapelle, A.
see Jensen, J. M. et al. see Huopaniemi, L. ef al.
chromosome 5q11—-13. New DNA markers with increased denaturing high performance liquid chromatography.
informativeness show diminished support for a... Superiority of... over single-stranded conformation
schizophrenia susceptibility locus and exlude linkage and conformation-sensitive gel electrophoresis for
in two new cohorts of British and Icelandic familes, mutation detection in TSC2, 383
230 dendritic cell marker. The human...CD83 maps to
chromosome 6p23. The human dendritic cell marker chromosome 6p23, 181
CD83 maps to, 181 Denmark. WUC7 gene polymorphism does not explain
Chromosome 9 Workshop. Report on the 1998 Inter- the different incidence of gastric cancer in Portugal
national, 101; Workshop Abstracts, 119; Addresses and, 187
of Participants, 125 Derenko, M.V
Ciclitira, P. J. S€¢ Malyarchuk, B. A.
see Brett, P. M. et al. De Wildt. S.C. M.
Clot. F. see Meulenbelt. I. et al.
see Giordano, M. ef al. Dey, C.
coeliac disease. Common HLA alleles, rather than rare see Bergen, A. W. ef al.
mutants, confer susceptibility to, 217 Dissing, J.
coeliac disease. Linkage disequilibrium between intra- Se€ Simonsen, K. et al.
locus variants in the aminopeptidase n gene and test Donner, A.
of their association with, 207 SeE Bartfay, E. et al.
Cohen, J. dopamine D2 receptor gene. Supportive evidence for
see Wang, J. contribution of the...to heritability of stature:
Cohen, J. linkage and association studies, 147
see Wang. J. et al. Dousset, B.
COL2A1 gg ene. Haplotype analysis of three poly- see Alif, N. et al
morphisms of the.. .and associations with general Doyle, E.
ised radiological osteoarthritis, 393 Se€E€ Klein. : et al.
Index
Du Toit, E. D. genome searches. Meta-analysis of, 263
see Pang, H. et al. Germany. Search for the PARK3 founder haplotype in a
dystonic patients. Detailed haplotype analysis in large cohort of patients with Parkinson's disease
Ashkenazi Jewish and non-Jewish British ... carry from Northern. 285
ing the GAG deletion in the DYTI gene: evidence Gersen, S. L. & Keagle. M. B.. eds
for a limited number of founder mutations, 1 The Principle s of Clinical Cytogenetics. reviewed by R
DYT1 gene. Detailed haplotype analysis in Ashkenazi Hall, 378
Jewish and non-Jewish British dystonic patients Giordano, M.. Bolognesi. E.. D’alfonso. S.. Lessi, M
carrying the GAG deletion in the ...: evidence for a Zavattari,. P.. Oderda. G.. Clot. F Percopo, ey
limited number of founder mutations, f Casari, G.. Greco. L Tosi. R. & Momigliano
Richiardi, P
Eckfeldt, J. H. linkage disequilibrium between intra-locus variants
see Coon, H. ef al. in the aminopeptidase n gene and test of their as
Edwards, J. H. sociation with coeliac disease, 207
see Chadwick et al. elucose-6 phosphatase gene Enz matic characterization
Elston, R. C. of four new mutations in the... which cause glycogen
see Guo, X. et al. storage disease type la mutations, 141
Erdmann, J., Riedel, K.. Rohde. K., Folgmann. | glycogen storage disease type la. Enzymatic character
Wienker. T.. Fleck, E. & Regitz-Zagrosek. V. ization of four new mutations in the glucose 6
characterization of polymorphisms in the promoter of phosphatase gene which cause, 141
the human angiotensin II subtype 1 (ATI) receptor Goldman, D.
gene, 369 see Bergen, A. W. ef al
Eriksson, A. (,omes Be Collins. A., Lonjou, C., Thomas
see Huopaniemi, L. ef al. Wilkinson, J... Watson, M. & Morton, N. E
European Mathematical Genetics Meeting Lough Hardy Weinberg quality control, 535
borough, April 1999. Abstracts of the, 351 Gonzalez. A. M
Ewens, W..J. see Rando, J.C. et al
see Grant, G. R. et al. Grant. G. R.. Manduchi. E Cheung. V.G. & Ewens.
W.J
Faergeman, O. significance testing for direct identityv-by-descent map
see Jensen, J. M. et al. ping, . 441
familial association of disease and the structure of rreco, L.
trivariate distributions. 539 see Giordano. M et al
Fellman, J. rroenmeijer, B. E
SeF Huopaniemi, L. et al. see Hallman, D. M etal
Ferrell, R. E. ruerra, R.
S€E Nelson. M. R. et al. see Wang. J. et al
Fleck, E tuo, X., Rotimi, C., Cooper. R Luke, A.. Elston, R. C
see Erdmann, J. etal Ogunbiyi, O. & Ward, R
Folgmann., I. evidence of a mayo! vene eftect for angiotensinogen
see Erdmann, J. ef al. among Nigerians 293
Forsius. H. Gurling. H.
see Huopaniemi, L. ef al. see Kalsi, G. et al
founder haplotype. Search for the PARK3...in a large
cohort of patients with Parkinson's disease from haemochromatosis. Rapid and simple determination of
Northern Germany, 285 hereditary ...m utations by multiplex PCR-SSCP
founder mutations. Detailed haplotype analysis in Detection of a new polymorphic mutation, 193
Ashkenazi Jewish and non-Jewish sritish dystonic Hagenah, JJ
patients carrying the GAG deletion in the DYTI see Klein, C ef al
gene: evidence for a limited number of, 1 Hall, F
Franz. D. see Choy, Y.S. et al
see Choy, Y.S. ef al. Hall, R.
fucosyltransferase gene (FU'76). Allelic diversity of the review of The Prine i ple s of Clinical Cytogenetics, edited
Q77 >
human |p lasma ((1.3). 277 by S. L. Gersen & M. B Keagle aid
Hallman, D. M Groenmeijer, B. E Jukema ‘ W
gamma frailty model. The additive genetic ... for linkage Boerwinkle, E & Kastelein, J.J. P
analysis, 455 analysis of lipoprotein lipase haplotypes reveals associ
Gardiner, M. ations not apparent from analysis of the constituent
review of Genetics of E pilepsies, edited by S. F loci, 499
Berkovic, P. Genton EK. Hirsch & F. Picard, 274 Hamaguchi H
Gasser, T. see Arinami,. T. ef al
see Klein, ¢ ‘etal. haploty pe analy sis. Detailed in Ashkenazi Jewish and
gastric cancer. MUC1 gene polymorphism does not non-Jewish British dystonic patients carrying the
explain the different incidence of ...in Portugal and GAG deletion in the DYTI vene evidence tor a
Denmark, 187 limited number of founder mutations, 1
IV Index
haplotype analysis of three polymorphisms of the Ishiguro, H.
COL2A1 gene and associations with generalised see Arinami, T. ef al.
radiological osteoarthritis, 39% 3 Ishikawa H.
Hardy-Weinberg quality control, 535 see Arinami, T. et al.
Harper, J. ed.
Skin Disorders: The Genodermatoses, reviewed by C.S. Jackson, C. L.
Munro, 567 see Chadwick, B. P. et al.
Hayer, M., Boenisch, H. & Bruess, M. Jacobs. H.
molecular cloning, functional characterization and see Klein, C. et al.
genomic organization of four alternatively spliced Japanese. Molecular scanning for mutations in the
isoforms of the human organic cation transporter 1! melanocortin-4 receptor gene in obese/diabetic, 483
(hOCT1/SLC22A 1), 473 Jefferson, K.
Heiss, G. see Bergen, A. W. et al.
see Coon, H. et al. Jensen, H. K.
Heng. C. K., Saha, N. & Low, P.S. see Jensen, J. M. et al.
evolution of the apolipoprotein B gene and coronary Jensen, J.M., Kruse, T. A.. Brorholt-Petersen, J. U..
artery disease: a study in low and high risk Asians, Christiansen, T. M., Jensen, H. K., Kolvraa, S. &
45 Faergeman, O.
Hernandez, M. linking genotype to aorto-coronary atherosclerosis: a
see Rando, J.C. et al. model using familial hypercholesterolemia and aorto-
Hess, K. coronary calcification, 511
sce Alif, N. et al. Jimenez, C.
HLA alleles. Common... . rather than rare mutants, review of In Situ Hybridization: A Practical Approach,
edited by D. G. Wilkinson, 379
confer susceptibility to coeliac disease, 217
Jones, T.
HLA class II genes. Locus and population specific
see Berchtold, 8. et al.
evolution in, 27
Jukema, J. W.
Hoelzel. A. R., ed
see Hallman, D. M. et al.
Molecular Genetic Analysis of Populations, reviewed
by J. Mallet, 273
Kalsi, G.. Mankoo, B., Curtis. D., Sherrington, R.,
Hofman, A.
Melmer,G. , Brynjolfsson, J.,Sigmundsson, T.. Read,
see Meulenbelt, I. el al.
T., Murphy. P., Petursson, H. & Gurling, H.
Hopkinson, D. A.
new DNA markers with increased informativeness
see Yip, S. P. et al.
show diminished support for a chromosome 5q11—-13
Humphries, 8. E.
schizophrenia susceptibility locus and exlude linkage
review of Evolution in Health and Disease, edited by
in two new cohorts of British and Icelandic familes,
S. C. Stearns, 274
235
Humphries, 8. E.
Karasik. D.
review of Evolutionary Aspects of Nutrition and Health:
see Livshits, G. et al.
Diet, Exercise, Genetics and Chronic Disease. edited
Kardia, S. L. R.
by A. P. Simopoulos, 377
see Nelson, M. R. et al.
Hunt, 8. C.
Kasprzyk-Obara, J.
see Coon, H. ef al.
see Choy, Y.S. et al.
Huopaniemi, L., Fellman, J.. Rantala, A., Eriksson, A.,
Kastelein, J.J. P.
Forsius, H., De La Chapelle, A. & Alitalo, T. see Hallman, D. M. ef al.
skewed secondary sex ratio in the offspring of carriers
Kidd J. R.
of the 214G A mutation of the RS1 gene, 521 see Quintana-Murci, L. et al.
Hurler syndrome. Mucopolysaccharidosis type I: charac- Kidd, J. R.
terization of a common mutation that causes...i n see Zhao. H. el al,
Moroccan subjects, 9 Kidd, K. K.
Hutchinson, T. P. see Zhao. H. et al.
familial association of disease and the structure of Kilker, R. L.
trivariate distributions, 539 see Li, W.-D. et al.
hypercholesterolemia. Linking genotype to aorto- Kimura, H.
coronary atherosclerosis: a model using familial ... see Pang. H. ef al.
and aorto-coronary calcification, 511 Klar, N.
see Bartfay. E. et al.
Icelandic families. New DNA markers with increased Klein, C., Vieregge, P.. Hagenah, J., Sieberer, M., Doyle,
informativeness show diminished support for a E.. Jacobs, H.. Gasser, T., Breakefield, X. O.., Risch.
chromosome 5q1| 1—-13 schizophrenia susceptibility: N. J. & Ozelius, L. J.
locus and exlude linkage in two new cohorts of search for the PARK3 founder haplotype in a large
British and, 235 cohort of patients with Parkinson's disease from
identity-by-descent mapping. Significance testing for Northern Germany, 285
direct, 441 Koda. YY.
lijima, Y. see Pang H. et al.
see Arinami, T. et al. Kolvraa, S.
Index
see Jensen, J. M. et al. see Quintana-Murci, L et al
Kronenberg, F. Maire I.
see Coon, H. et al. see Bruni, N el al
Kruse, T. A. Mallet, J.
see Jensen, J. M. et al. review of Molecular Genetic Analysis of Populations
Kwiatkowski, D. J. edited by A. R. Hoelzel, 273
See Choy, Y.S. et al Malvarchuk, B. A. & Derenko, M. V
molecular instability of the mitochondrial haplogroup T
Lanchbury, J.S sequences at nucleotide positions 16292 and 16296
see Wise, L. H et al. 489
Larruga, J. M. Manduchi, E.
see Rando, J. C. et al. see Grant. G. R. et al
LDL cholesterol. Evidence for a major gene accounting Mankoo B.
for mild elevation in...: The NHLBI Family Heart see Kalsi, G etal
Study, 401 Martinelli, M.
Lee, J. H. SeE¢ Scapoli, } et al
SE |a i, W.-D. et al. Meweeney, S. K
Leppert. M. F. see Valdes, A. M el al
see Coon, H. et al. melanocortin-4 receptor gene Molecular scanning tor
leptin gene. Sequence variants in the promotor and 5i mutations in the... n obese /diabetic Japanese, 483
untranslated region of the... are associated with Melmer, G.
obesity in women, 227 see Kalsi. G. et al
Lessi, M. meta-analysis of genome searches, 263
see Giordano, M. et al. Meulenbelt, I., Bijkerk, C., De Wildt, S.C. M Miedema
Lewis, C. M. H.S.. Breedveld, F. ¢ Pols, H. A P.. Hofman, A..
see Wise, L. H. et al. Van Duijn, C. M. & Slagboom, P. E
Li, H. haplotype analysis of three polymorphisms of the
the additive genetic gamma frailty model for linkage COL2A1 gene and associations with generalised
analysis, 455 radiological osteoarthritis. 393
i, W.-D., Reed, D. R., Lee, J. H., Xu, W., Kilker, R. L., Meyer, D.
Sodam, B. R. & Arlen Price, R. see Valdes, A. M. et al
sequence variants in the promotor and 51 untranslated microsatellite haplotyping. An Asian — Native American
region of the leptin gene are associated with obesity paternal lineage identified by RPS4Y resequencing
in women, 227 and by. 63
linkage. Supportive evidence for contribution of the Miedema, H.S.
dopamine D2 receptor gene to heritability of stature see Meulenbelt, | et al
.and association studies, 147 Mithieux, G.
linkage analysis. Power of variance component... to see Bruni. N. et al
detect quantitative trait loci, 545 mitochondrial haplogroup T sequences. Molecular in
linkage analysis. The additive genetic gamma frailty stability of... at nucleotide positions 16292 and
model for, 455 16296, 489
linkage analysis. Combined segregation and...o f non Momigliano Richiardi, P
syndromic orofacial cleft in two candidate regions. see Giordano, M. ef al
17 Montano, S.
linkage disequilibrium. Assessing ... in a complex genetic see Bruni, N. et al
system. I. Overall linkage disequilibrium, 167 Morocean subjects. Mucopolysaccharidosis type |
linkage disequilibrium between intra-locus variants in characterization of a common mutation that causes
the aminopeptidase n gene and test of their as Hurler syndrome in, 9
sociation with coeliac disease, 207 Morris. M-A
lipoprotein lipase. Analysis of ... haplotypes reveals asso see Brett, P. M. et al
ciations not apparent from analysis of the con Morton, N. E
stituent loci, 499 see Gomes, I. et al
Liu, A. mtDNA. Phylogeographi« patterns of... reflecting the
see Quintana-Murci, L. et al. colonization of the Canary Islands, 413»
Livshits. G., Karasik, D. & Seibel. M. J. MUC1 gene polymorphism does not explain the different
statistical genetic analysis of plasma levels of vitamin incideofn gcasetri c cancer in Portugaaln d Denmark,
D: familial study., 429 187
Lonjou, C. mucopoly saccharidosis t\ pe | characterization of a
see Gomes, IL. et al. common mutation that causes Hurler syndrome in
Low, P.S. Moroccan subjects, 9
see Heng, C. K. et al. Muhl-Zurbes, P.
Luke, A. see Berchtold. S et al
see Guo, X. et al. multiplex PCR-SSCP. Rapid and simple determination
of hereditary haemochromatosis mutations by ...
Maccioni, L. Detection of a new polymorphic mutation, 193
vi Index
Munro, C.S. Pakstis, A. J.
review of Skin Disorders The Genodermatoses. edited see Zhao. H. et al.
by J. Harper, 567 Pang. H., Koda, Y., Soejima, M., Schlaphoff, T., Du
Murphy, P. Toit. E. D. & Kimura, H
see Kalsi. G. et al. allelic diversity of the human plasma ((1,3)fucosyl-
mutation detection in TSC2. Superiority of denaturing transferase gene (FUT6), 277
high performance liquid chromatography over Parkinson's disease. Search for PARK3 founder haplo-
single-stranded conformation and conformation- type in a large cohort of patients with... from
sensitive gel electrophoresis for, 383 Northern Germany, 285
Myers, R. H. Passarino, G.
see Coon, H. et al, see Quintana-Murci, L. ef al.
paternal lineage. An Asian-Native American ... identified
Nabet. P. by RPS4Y resequencing and by microsatellite haplo-
see Alif. N. et al. typing, 63
Nakagawa. T. Peixoto, A.
see Ohshiro, Y. el al. see Carvalho, F. et al.
Nanjo. K. Percopo, 8.
see Ohshiro, Y. et al. see Giordano. M. et al.
Native American. An Asian ... paternal lineage identi- Petursson, H.
fied by RPS4Y resequencing and by microsatellite see Kalsi, G. et al.
haplotyping, 63 Pezzetti. F.
N’bou. A. see Scapoli, C. et al.
see Alif. N. et al. phosphoglucomutase (PGM1). Identification and charac-
Nelson. M. P. terisation of polymorphisms in human, 129
see Valdes. A. M. et al. Pinto, F.
Nelson. M. R., Kardia. S. L R.. Ferrell, R. E. & Sing. see Rando, J. C. et al.
CG; i. Poloni, E.S.
influence of apolipoprotein E genotype variation on the see Quintana-Murci, L. ef al.
means, variances, and correlations of plasma lipids Pols, H. A. P.
and apolipoproteins in children, 311 see Meulenbelt, 1. et al.
NHLBI Family Heart Study Evidence for a major gene population specific evolution. Locus and ...in HLA class
accounting for mild elevation in LDL cholesterol: I] genes, 27
401 Portugal. WUC1 gene polymorphism does not explain
Nigerians. Evidence of a major gene effect for angio the different incidence of gastric cancer in... and
tensinogen among. 293 Denmark. 187
Niida,. Y. Povey 8.
see Choy. Y.S. et al. see Chadwick. B. P. et al.
Povey, 8.
obese/diabetic. Molecular scanning for mutations in the see Valente. E. M. et al.
melanocortin-4 receptor gene in... Japanese, 483 Province, M. A.
obesity. Sequence variants in the promotor and 5’ see Coon. H. ef al.
untranslated region of the leptin gene are associated Putt. W.
with...in women, 227 S@¢ Yip. S. P. et al.
Oderda, G.
see Giordano, M. ef al. quantitative trait linkage analysis. A statistically robust
Ogunbiyi, O. variance component approach for, 249
SéE Guo. aS et al. quantitative trait loci. A correction to TDT statistics for
Ohshiro, Y.. Sanke. T.. Ueda. K.. Shimajiri. Y.. mapping, 469
Nakagawa. T.. Tsunoda. K. & Nanjo, K. quantitative trait loci. Power of variance component
molecular scanning for mutations in the melanocortin linkage analysis to detect, 545
4 receptor gene in obese/diabetic Japanese, 483 Quintana-Murei, L.. Semino, O.. Poloni, E.S., Liu, A.,
Ohtsuki, T. Van Gijn, M., Passarino, G., Brega, A., Maccioni, L..
see Arinami, T. ef al. Cossu, G.. Al-Zahery, N., Kidd J. R. & Santachiara-
organic cation transporter | (OCTL/SLC22A1). Molecular Benerecetti ALS.
cloning, functional characterization and genomic Y-chromosome specific YCATT, DYS19 and YAP poly-
organization of four alternatively spliced isoforms of morphisms in human populations: a comparative
the human, 473 study, 153
orofacial cleft. Combined segregation and linkage analysis
of nonsyndromic ...in two candidate regions, 17 Rajas. F.
osteoarthritis. Haplotype analysis of three polymorph- see Bruni, N. et al,
isms of the COL2A1 gene and associations with tamesh,. V.
2Q%
generalised radiological 393 SOE Choy. Y.S. et al.
Ozelius, L. J. Rando, J. C.. Cabrera, V. M., Larruga. J. M.. Hernandez,
see Chadwick. B. P. et al. M.. Gonzalez, A. M., Pinto, F. & Bandelt. H.-J.
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