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Human Genetics|December 14, 2004
Association of alpha2-HS glycoprotein (AHSG, fetuin-A) polymorphism with AHSG and phosphate serum levelsMotoki Osawa, Wei Tian, Hidekazu Horiuchi, et al.Human Genetics|July 17, 2004
CHX10 mutations cause non-syndromic microphthalmia/ anophthalmia in Arab and Jewish kindredsUdy Bar-Yosef, Izzeldin Abuelaish, Tamar Harel, et al.Human Genetics|October 31, 1978
Rapid identification of chromosomes carrying silver-stained nucleolus-organizing regions: application to case of 21/21 Robertsonian translocationC H Buys, J Osinga, W L Gouw, et al.Human Genetics|July 3, 2004
Directional migration in the Hindu castes: inferences from mitochondrial, autosomal and Y-chromosomal dataStephen Wooding, Christopher Ostler, B V Ravi Prasad, et al.Human Genetics|July 3, 2004
Chromosome 17p12-q11 harbors susceptibility loci for systemic lupus erythematosusCecilia M Johansson, Renata Zunec, Mercedes A García, et al.Human Genetics|June 9, 2004
Interaction effect of PTEN and CDKN1B chromosomal regions on prostate cancer linkageJianfeng Xu, Carl D Langefeld, S Lilly Zheng, et al.Human Genetics|May 10, 1977
Three glucose 6-phosphate dehydrogenase variants found in JapanS H Miwa, K Nakashima, J Ono, et al.Human Genetics|July 26, 2005
Heightened stress response in primary fibroblasts expressing mutant eIF2B genes from CACH/VWM leukodystrophy patientsLiraz Kantor, Heather P Harding, David Ron, et al.Human Genetics|June 29, 2005
A systematic analysis of LINE-1 endonuclease-dependent retrotranspositional events causing human genetic diseaseJian-Min Chen, Peter D Stenson, David N Cooper, et al.Human Genetics|June 1, 2005
Monozygous triplets discordant for transient neonatal diabetes mellitus and for imprinting of the TNDM differentially methylated regionS G Kant, A M van der Weij, W Oostdijk, et al.Pageof 957