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American Journal of Human Genetics|December 1, 1993
Independent origin of identical beta cardiac myosin heavy-chain mutations in hypertrophic cardiomyopathyH Watkins, L Thierfelder, R Anan, et al.American Journal of Human Genetics|December 1, 1993
Pedigree models for complex human traits involving the mitochondrial genomeN J Schork, S W GuoAmerican Journal of Human Genetics|December 1, 1993
Conclusions of segregation analysis for family data generated under two-locus modelsM H Dizier, C Bonaïti-Pellié, F Clerget-DarpouxAmerican Journal of Human Genetics|May 7, 2002
Founding mothers of Jewish communities: geographically separated Jewish groups were independently founded by very few female ancestorsMark G Thomas, Michael E Weale, Abigail L Jones, et al.American Journal of Human Genetics|May 7, 2002
Minimum-recombinant haplotyping in pedigreesDajun Qian, Lars BeckmannAmerican Journal of Human Genetics|May 7, 2002
Mutations in COL6A3 cause severe and mild phenotypes of Ullrich congenital muscular dystrophyErcan Demir, Patrizia Sabatelli, Valérie Allamand, et al.American Journal of Human Genetics|May 7, 2002
Patterns of meiotic recombination in human fetal oocytesCharles Tease, Geraldine M Hartshorne, Maj A HulténAmerican Journal of Human Genetics|May 7, 2002
Genomewide comparison of DNA sequences between humans and chimpanzeesIngo Ebersberger, Dirk Metzler, Carsten Schwarz, et al.American Journal of Human Genetics|October 1, 1992
Genotype-phenotype relationships in human red/green color-vision defects: molecular and psychophysical studiesS S Deeb, D T Lindsey, Y Hibiya, et al.American Journal of Human Genetics|November 1, 1992
Localization of the photoreceptor gene ROM1 to human chromosome 11 and mouse chromosome 19: sublocalization to human 11q13 between PGA and PYGMR A Bascom, J García-Heras, C L Hsieh, et al.Pageof 981