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American Journal of Human Genetics|September 1, 1979
Congenital universal muscular hypoplasia: evidence for autosomal recessive inheritanceM Z Pelias, T F ThurmonAmerican Journal of Human Genetics|September 1, 1975
Functional implications of differential chromosome bandingH HoehnAmerican Journal of Human Genetics|May 1, 1979
Familial hyperlysinemia: enzyme studies, diagnostic methods, comments on terminologyJ Dancis, J Hutzler, R P CoxAmerican Journal of Human Genetics|May 1, 1979
Hemolytic anemia due to pyruvate kinase deficiency: characterization of the enzymatic activity from eight patientsJ A Black, M B Rittenberg, R H Bigley, et al.American Journal of Human Genetics|March 1, 1979
Genetic drift in sex-linked lethal disordersM Slatkin, G Thomson, S SawyerAmerican Journal of Human Genetics|March 1, 1979
Maximum likelihood estimation by counting methods under polygenic and mixed models in human pedigreesJ OttAmerican Journal of Human Genetics|March 1, 1979
Familial X-linked mental retardation, verbal disability, and marker X chromosomesP N Howard-Peebles, G R Stoddard, M G MimsAmerican Journal of Human Genetics|January 25, 2022
Midbrain organoids mimic early embryonic neurodevelopment and recapitulate LRRK2-p.Gly2019Ser-associated gene expressionAlise Zagare, Kyriaki Barmpa, Semra Smajic, et al.American Journal of Human Genetics|March 1, 1988
Efficient computations in multilocus linkage analysisG M Lathrop, J M LalouelAmerican Journal of Human Genetics|October 6, 2018
Mutations in KCNK4 that Affect Gating Cause a Recognizable Neurodevelopmental SyndromeChristiane K Bauer, Paolo Calligari, Francesca Clementina Radio, et al.Pageof 979