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American Journal of Human Genetics|January 1, 1977
Structure and Barr body formation of an Xp + chromosome with two inactivation centersR F Daly, K Patau, E Therman, et al.
American Journal of Human Genetics|April 23, 2019
Conformational Dynamics and Allosteric Regulation Landscapes of Germline PTEN Mutations Associated with Autism Compared to Those Associated with CancerIris Nira Smith, Stetson Thacker, Marilyn Seyfi, et al.
American Journal of Human Genetics|November 8, 2003
Predisposition locus for major depression at chromosome 12q22-12q23.2Victor Abkevich, Nicola J Camp, Charles H Hensel, et al.
American Journal of Human Genetics|December 1, 1992
Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndromeN G Larsson, M H Tulinius, E Holme, et al.
American Journal of Human Genetics|December 1, 1992
The gender-specific apolipoprotein E genotype influence on the distribution of plasma lipids and apolipoproteins in the population of Rochester, Minnesota. II. Regression relationships with concomitantsS L Reilly, R E Ferrell, B A Kottke, et al.
American Journal of Human Genetics|December 1, 1992
Characteristics of polymorphism at a VNTR locus 3' to the apolipoprotein B gene in five human populationsR Deka, R Chakraborty, S DeCroo, et al.
American Journal of Human Genetics|December 1, 1992
The gene for familial Mediterranean fever in both Armenians and non-Ashkenazi Jews is linked to the alpha-globin complex on 16p: evidence for locus homogeneityM Shohat, X Bu, T Shohat, et al.
American Journal of Human Genetics|October 21, 2003
Germline inactivation of PTEN and dysregulation of the phosphoinositol-3-kinase/Akt pathway cause human Lhermitte-Duclos disease in adultsXiao-Ping Zhou, Deborah J Marsh, Carl D Morrison, et al.
American Journal of Human Genetics|September 19, 2003
A genomewide screen of 345 families for autism-susceptibility lociAmanda L Yonan, Maricela Alarcón, Rong Cheng, et al.
American Journal of Human Genetics|January 1, 1992
Two amino acid substitutions in apolipoprotein B are in complete allelic association with the antigen group (x/y) polymorphism: evidence for little recombination in the 3' end of the human geneA M Dunning, H H Renges, C F Xu, et al.
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