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American Journal of Human Genetics|January 1, 1992
Mucolipidoses II and III variants with normal N-acetylglucosamine 1-phosphotransferase activity toward alpha-methylmannoside are due to nonallelic mutationsY Ben-Yoseph, D A Mitchell, R M Yager, et al.
American Journal of Human Genetics|May 9, 2003
Genomewide scan for hand osteoarthritis: a novel mutation in matrilin-3Stefán Einar Stefánsson, Helgi Jónsson, Thorvaldur Ingvarsson, et al.
American Journal of Human Genetics|December 1, 1992
Cleft lip with or without cleft palate: associations with transforming growth factor alpha and retinoic acid receptor lociG Chenevix-Trench, K Jones, A C Green, et al.
American Journal of Human Genetics|December 11, 1992
Improved predictive test for MEN2, using flanking dinucleotide repeats and RFLPsJ R Howe, T C Lairmore, S K Mishra, et al.
American Journal of Human Genetics|August 1, 1992
Expected behavior of conditional linkage disequilibriumN Kaplan, B S Weir
American Journal of Human Genetics|May 1, 1992
Confirmation and refinement of the genetic localization of the Coffin-Lowry syndrome locus in Xp22.1-p22.2V Biancalana, M L Briard, A David, et al.
American Journal of Human Genetics|July 19, 2003
Phylogeny of east Asian mitochondrial DNA lineages inferred from complete sequencesQing-Peng Kong, Yong-Gang Yao, Chang Sun, et al.
American Journal of Human Genetics|February 12, 2011
Hexosamine biosynthetic pathway mutations cause neuromuscular transmission defectJan Senderek, Juliane S Müller, Marina Dusl, et al.
American Journal of Human Genetics|February 8, 2011
Functional screening of Alzheimer pathology genome-wide association signals in DrosophilaJoshua M Shulman, Portia Chipendo, Lori B Chibnik, et al.
American Journal of Human Genetics|February 8, 2011
Ancient voyaging and Polynesian originsPedro Soares, Teresa Rito, Jean Trejaut, et al.
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