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American Journal of Human Genetics|February 12, 2004
Homozygous WNT3 mutation causes tetra-amelia in a large consanguineous familyStephan Niemann, Chengfeng Zhao, Filon Pascu, et al.
American Journal of Human Genetics|May 22, 2004
Whole-genome scan, in a complex disease, using 11,245 single-nucleotide polymorphisms: comparison with microsatellitesSally John, Neil Shephard, Guoying Liu, et al.
American Journal of Human Genetics|May 22, 2004
Allelic heterogeneity in the COH1 gene explains clinical variability in Cohen syndromeHans Christian Hennies, Anita Rauch, Wenke Seifert, et al.
American Journal of Human Genetics|May 22, 2004
A common haplotype of the nicotine acetylcholine receptor alpha 4 subunit gene is associated with vulnerability to nicotine addiction in menYan Feng, Tianhua Niu, Houxun Xing, et al.
American Journal of Human Genetics|April 29, 2005
Alternative splicing suggests extended function of PEX26 in peroxisome biogenesisSabine Weller, Ivelisse Cajigas, James Morrell, et al.
American Journal of Human Genetics|March 26, 2005
Increased level of linkage disequilibrium in rural compared with urban communities: a factor to consider in association-study designVeronique Vitart, Andrew D Carothers, Caroline Hayward, et al.
American Journal of Human Genetics|March 11, 2005
Single- and multilocus allelic variants within the GABA(B) receptor subunit 2 (GABAB2) gene are significantly associated with nicotine dependenceJoke Beuten, Jennie Z Ma, Thomas J Payne, et al.
American Journal of Human Genetics|May 1, 1992
Familial case with sequence variant in the testis-determining region associated with two sex phenotypesE Vilain, K McElreavey, F Jaubert, et al.
American Journal of Human Genetics|May 1, 1992
Multipoint linkage analysis in Menkes diseaseT Tønnesen, A Petterson, T A Kruse, et al.
American Journal of Human Genetics|May 1, 1992
Band-specific localization of the microsatellite at D13S71 by microdissection and enzymatic amplificationH Spielvogel, H C Hennies, U Claussen, et al.
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