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American Journal of Human Genetics|March 26, 1999
Age estimates of two common mutations causing factor XI deficiency: recent genetic drift is not necessary for elevated disease incidence among Ashkenazi JewsD B Goldstein, D E Reich, N Bradman, et al.American Journal of Human Genetics|March 26, 1999
Low-copy repeats mediate the common 3-Mb deletion in patients with velo-cardio-facial syndromeL Edelmann, R K Pandita, B E MorrowAmerican Journal of Human Genetics|March 26, 1999
Analysis of chromosome 1q42.2-43 in 152 families with high risk of prostate cancerM Gibbs, L Chakrabarti, J L Stanford, et al.American Journal of Human Genetics|March 26, 1999
Delineation of the critical deletion region for congenital heart defects, on chromosome 8p23.1K Devriendt, G Matthijs, R Van Dael, et al.American Journal of Human Genetics|March 26, 1999
Linkage of type 2 diabetes mellitus and of age at onset to a genetic location on chromosome 10q in Mexican AmericansR Duggirala, J Blangero, L Almasy, et al.American Journal of Human Genetics|March 26, 1999
Comparison of linkage-disequilibrium methods for localization of genes influencing quantitative traits in humansG P Page, C I AmosAmerican Journal of Human Genetics|November 4, 2000
Family-based tests of association in the presence of linkageS L Lake, D Blacker, N M LairdAmerican Journal of Human Genetics|November 4, 2000
Complex segregation analysis provides compelling evidence for a major gene underlying obsessive-compulsive disorder and for heterogeneity by sexG Nestadt, T Lan, J Samuels, et al.American Journal of Human Genetics|November 15, 2000
Mutations in FOXC2 (MFH-1), a forkhead family transcription factor, are responsible for the hereditary lymphedema-distichiasis syndromeJ Fang, S L Dagenais, R P Erickson, et al.American Journal of Human Genetics|November 15, 2000
The IBD2 locus shows linkage heterogeneity between ulcerative colitis and Crohn diseaseM Parkes, M M Barmada, J Satsangi, et al.Pageof 981