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Table of contents of journal: *Annals of human genetics

Results: 101-125/405

Authors: Klein, C Vieregge, P Hagenah, J Sieberer, M Doyle, E Jacobs, H Gasser, T Breakefield, XO Risch, NJ Ozelius, LJ
Citation: C. Klein et al., Search for the PARK3 founder haplotype in a large cohort of patients with Parkinson's disease from Northern Germany, ANN HUM GEN, 63, 1999, pp. 285-291

Authors: Guo, X Rotimi, C Cooper, R Luke, A Elston, RC Ogunbiyi, O Ward, R
Citation: X. Guo et al., Evidence of a major gene effect for angiotensinogen among Nigerians, ANN HUM GEN, 63, 1999, pp. 293-300

Authors: Corbo, RM Scacchi, R
Citation: Rm. Corbo et R. Scacchi, Apolipoprotein E (APOE) allele distribution in the world. Is APOE4 a 'thrifty' allele?, ANN HUM GEN, 63, 1999, pp. 301-310

Authors: Nelson, MR Kardia, SLR Ferrell, RE Sing, CF
Citation: Mr. Nelson et al., Influence of apolipoprotein E genotype variation on the means, variances, and correlations of plasma lipids and apolipoproteins in children, ANN HUM GEN, 63, 1999, pp. 311-328

Authors: Waldman, ID Robinson, BF Rowe, DC
Citation: Id. Waldman et al., A logistic regression based extension of the TDT for continuous and categorical traits, ANN HUM GEN, 63, 1999, pp. 329-340

Authors: Bartfay, E Donner, A Klar, N
Citation: E. Bartfay et al., Testing the equality of twin correlations with multinomial outcomes, ANN HUM GEN, 63, 1999, pp. 341-349

Citation: European Mathematical Genetics Meeting held at Loughborough, 9-11 April 1999 - Abstracts, ANN HUM GEN, 63, 1999, pp. 351-367

Authors: Erdmann, J Riedel, K Rohde, K Folgmann, I Wienker, T Fleck, E Regitz-Zagrosek, V
Citation: J. Erdmann et al., Characterization of polymorphisms in the promoter of the human angiotensinII subtype 1 (AT1) receptor gene, ANN HUM GEN, 63, 1999, pp. 369-374

Authors: Carvalho, F Peixoto, A Steffensen, R Amorim, A David, L Sobrinho-Simoes, M
Citation: F. Carvalho et al., MUC1 gene polymorphism does not explain the different incidence of gastriccancer in Portugal and Denmark, ANN HUM GEN, 63, 1999, pp. 187-191

Authors: Simonsen, K Dissing, J Rudbeck, L Schwartz, M
Citation: K. Simonsen et al., Rapid and simple determination of hereditary haemochromatosis mutations bymultiplex PCR-SSCP: detection of a new polymorphic mutation, ANN HUM GEN, 63, 1999, pp. 193-197

Authors: Abulhasan, SJ Tayel, SM Al-Awadi, SA
Citation: Sj. Abulhasan et al., Mosaic Turner syndrome: cytogenetics versus FISH, ANN HUM GEN, 63, 1999, pp. 199-206

Authors: Giordano, M Bolognesi, E D'Alfonso, S Lessi, M Zavattari, P Oderda, G Clot, F Percopo, S Casari, G Greco, L Tosi, R Momigliano-Richiardi, P
Citation: M. Giordano et al., Linkage disequilibrium between intra-locus variants in the aminopeptidase n gene and test of their association with coeliac disease, ANN HUM GEN, 63, 1999, pp. 207-215

Authors: Brett, PM Yiannakou, JY Morris, MA Vaughan, R Curtis, D Ciclitira, PJ
Citation: Pm. Brett et al., Common HLA alleles, rather than rare mutants, confer susceptibility to coeliac disease, ANN HUM GEN, 63, 1999, pp. 217-225

Authors: Li, WD Reed, DR Lee, JH Xu, W Kilker, RL Sodam, BR Price, RA
Citation: Wd. Li et al., Sequence variants in the 5 ' flanking region of the leptin gene are associated with obesity in women, ANN HUM GEN, 63, 1999, pp. 227-234

Authors: Kalsi, G Mankoo, B Curtis, D Sherrington, R Melmer, G Brynjolfsson, J Sigmundsson, T Read, T Murphy, P Petersson, H Gurling, H
Citation: G. Kalsi et al., New DNA markers with increased informativeness show diminished support fora chromosome 5q11-13 schizophrenia susceptibility locus and exclude linkage in two new cohorts of British and Icelandic families, ANN HUM GEN, 63, 1999, pp. 235-247

Authors: Wang, J Guerra, R Cohen, J
Citation: J. Wang et al., A statistically robust variance-components approach for quantitative traitlinkage analysis, ANN HUM GEN, 63, 1999, pp. 249-262

Authors: Wise, LH Lanchbury, JS Lewis, CN
Citation: Lh. Wise et al., Meta-analysis of genome searches, ANN HUM GEN, 63, 1999, pp. 263-272

Authors: Bode, J Bartsch, J Benham, C Janusch, H Knopp, A Olopade, F Schon, O Seibler, J Strissel, P
Citation: J. Bode et al., Sixth international workshop on chromosome 9 - Abstracts, ANN HUM GEN, 63, 1999, pp. 119-124

Authors: Yip, SP Putt, W Hopkinson, DA Whitehouse, DB
Citation: Sp. Yip et al., Identification and characterisation of polymorphisms in human phosphoglucomutase (PGM1), ANN HUM GEN, 63, 1999, pp. 129-140

Authors: Bruni, N Rajas, F Montano, S Chevalier-Porst, F Maire, I Mithieux, G
Citation: N. Bruni et al., Enzymatic characterization of four new mutations in the glucose-6 phosphatase (G6PC) gene which cause glycogen storage disease type 1a, ANN HUM GEN, 63, 1999, pp. 141-146

Authors: Arinami, T Iijima, Y Yamakawa-Kobayashi, K Ishiguro, H Ohtsuki, T Yanagi, H Shimakura, Y Ishikawa, H Hamaguchi, H
Citation: T. Arinami et al., Supportive evidence for contribution of the dopamine D2 receptor gene to heritability of stature: linkage and association studies, ANN HUM GEN, 63, 1999, pp. 147-151

Authors: Quintana-Murci, L Semino, O Poloni, ES Liu, A Van Gijn, M Passarino, G Brega, A Nasidze, IS Maccioni, L Cossu, G Al-Zahery, N Kidd, JR Kidd, KK Santachiara-Benerecetti, AS
Citation: L. Quintana-murci et al., Y-chromosome specific YCAII, DYS19 and YAP polymorphisms in human populations: a comparative study, ANN HUM GEN, 63, 1999, pp. 153-166

Authors: Zhao, H Pakstis, AJ Kidd, JR Kidd, KK
Citation: H. Zhao et al., Assessing linkage disequilibrium in a complex genetic system. I. Overall deviation from random association, ANN HUM GEN, 63, 1999, pp. 167-179

Authors: Berchtold, S Jones, T Muhl-Zurbes, P Sheer, D Schuler, G Steinkasserer, A
Citation: S. Berchtold et al., The human dendritic cell marker CD83 maps to chromosome 6p23, ANN HUM GEN, 63, 1999, pp. 181-183

Authors: Valente, EM Povey, S Warner, TT Wood, NW Davis, MB
Citation: Em. Valente et al., Detailed haplotype analysis in Ashkenazi Jewish and non-Jewish British dystonic patients carrying the GAG deletion in the DYT1 gene: evidence for a limited number of founder mutations, ANN HUM GEN, 63, 1999, pp. 1-8
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