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American Journal of Human Genetics|September 1, 1977
Maternal influence on plasma cholesterol variationJ C Christian, K W KangAmerican Journal of Human Genetics|September 1, 1977
Recombination, mutation, or constitutive expression at a Gm locus and familial hypergammaglobulinemiaG Lefranc, L Rivat, J P Salier, et al.American Journal of Human Genetics|December 1, 1996
Age and origin of two common MLH1 mutations predisposing to hereditary colon cancerA L Moisio, P Sistonen, J Weissenbach, et al.American Journal of Human Genetics|December 1, 1996
Familial transmission of the FMR1 CGG repeatS L Nolin, F A Lewis, L L Ye, et al.American Journal of Human Genetics|December 1, 1996
Severe and mild mutations in cis for the methylenetetrahydrofolate reductase (MTHFR) gene, and description of five novel mutations in MTHFRP Goyette, B Christensen, D S Rosenblatt, et al.American Journal of Human Genetics|December 1, 1996
Linkage-disequilibrium mapping narrows the Fukuyama-type congenital muscular dystrophy (FCMD) candidate region to <100 kbT Toda, M Miyake, K Kobayashi, et al.American Journal of Human Genetics|December 1, 1996
Using the expectation or the distribution of the identity by descent for mapping quantitative trait loci under the random modelD D Gessler, S XuAmerican Journal of Human Genetics|November 1, 1996
Gene structure and mutations of glutaryl-coenzyme A dehydrogenase: impaired association of enzyme subunits that is due to an A421V substitution causes glutaric acidemia type I in the AmishB J Biery, D E Stein, D H Morton, et al.American Journal of Human Genetics|November 1, 1996
Novel molecular variants of the Na-Cl cotransporter gene are responsible for Gitelman syndromeN Mastroianni, A Bettinelli, M Bianchetti, et al.American Journal of Human Genetics|November 1, 1996
Mild and severe muscular dystrophy caused by a single gamma-sarcoglycan mutationE M McNally, M R Passos-Bueno, C G Bönnemann, et al.Pageof 980