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American Journal of Human Genetics|October 7, 2008
A connective tissue disorder caused by mutations of the lysyl hydroxylase 3 geneAntti M Salo, Helen Cox, Peter Farndon, et al.American Journal of Human Genetics|July 1, 1991
Three different frameshift mutations of the tyrosinase gene in type IA oculocutaneous albinismW S Oetting, M M Mentink, C G Summers, et al.American Journal of Human Genetics|December 9, 2008
The genetic legacy of religious diversity and intolerance: paternal lineages of Christians, Jews, and Muslims in the Iberian PeninsulaSusan M Adams, Elena Bosch, Patricia L Balaresque, et al.American Journal of Human Genetics|August 1, 1991
Human beta-galactosidase gene mutations in GM1-gangliosidosis: a common mutation among Japanese adult/chronic casesK Yoshida, A Oshima, M Shimmoto, et al.American Journal of Human Genetics|June 1, 1991
Tyrosinase gene mutations associated with type IB ("yellow") oculocutaneous albinismL B Giebel, R K Tripathi, K M Strunk, et al.American Journal of Human Genetics|March 3, 2009
Genome-wide association and follow-up replication studies identified ADAMTS18 and TGFBR3 as bone mass candidate genes in different ethnic groupsDong-Hai Xiong, Xiao-Gang Liu, Yan-Fang Guo, et al.American Journal of Human Genetics|May 16, 2009
Genome-wide insights into the patterns and determinants of fine-scale population structure in humansShameek Biswas, Laura B Scheinfeldt, Joshua M AkeyAmerican Journal of Human Genetics|July 1, 1977
Human red cell 2,3-diphosphoglycerate mutase and monophosphoglycerate mutase: genetic evidence for two separate lociS H Chen, J E Anderson, E R GiblettAmerican Journal of Human Genetics|April 28, 2009
Significant linkage evidence for a predisposition gene for pelvic floor disorders on chromosome 9q21Kristina Allen-Brady, Peggy A Norton, James M Farnham, et al.American Journal of Human Genetics|July 7, 2009
Mutation in pyrroline-5-carboxylate reductase 1 gene in families with cutis laxa type 2Duane L Guernsey, Haiyan Jiang, Susan C Evans, et al.Pageof 979