Phylogenetic Relationships of Human Populations in Sub-Saharan Africa von WEBER, W., NASH, D.J., MOTULSKY, A.G., HENNEBERG, MACIEJ, CRAWFORD, MICHAEL H., MARTIN, S.K., GOLDSMID, J.M., SPEDINI, G., GLIDEWELL, S., SCHANFIELD, M. S.

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Update to "Metabolic Polymorphisms and the Role of Infectious Diseases in Human Evolution" von MOTULSKY, A.G.

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Myocardial infarction in the familial forms of hypertriglyceridemia von Brunzell, J.D., Schrott, H.G., Motulsky, A.G., Bierman, E.L.

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Genotype-phenotype relationships in human red/green color-vision defects : molecular and psychophysical studies von DEEB, S. S, LINDSEY, D. T, HIBIYA, Y, SANOCKI, E, WINDERICKX, J, TELLER, D. Y, MOTULSKY, A. G

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Severity of color vision defects: electroretinographic (ERG), molecular and behavioral studies von Crognale, M.A, Teller, D.Y, Motulsky, A.G, Deeb, S.S

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Analysis of red/green color discrimination in subjects with a single X-linked photopigment gene von Crognale, M.A, Teller, D.Y, Yamaguchi, T, Motulsky, A.G, Deeb, S.S

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Twenty-year cardiovascular disease mortality in the familial forms of hypertriglyceridemia von Austin, M.A., McKnight, B., Edwards, K.L., Bradley, C.M., McNeely, M.J., Psaty, B.M., Brunzell, J.D., Motulsky, A.G.

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Molecular Genetics of X Chromosome-Linked Color Vision Among Populations of African and Japanese Ancestry: High Frequency of a Shortened Red Pigment Gene Among Afro-Americans von Jørgensen, A. Lund, Deeb, S. S., Motulsky, A. G.

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Nutrition and genetic susceptibility to common diseases von Motulsky, AG

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Erythrocyte carbohydrate metabolism in hereditary hemolytic anemias von Motulsky, A.G., Gabrio, B.W., Burkhardt, J., Finch, C.A.

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The 1985 Nobel Prize in Physiology or Medicine von Motulsky, A. G.

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Molecular patterns of X chromosome-linked color vision genes among 134 menof European ancestry von Drummond-Borg, M., Deeb, S.S., Motulsky, A.G.

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Impact of Genetic Manipulation on Society and Medicine von Motulsky, Arno G.

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Human genetic variation and nutrition von Motulsky, A G

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Chromosomal Localization of the Human Apolipoprotein B Gene and Detection of Homologous RNA in Monkey Intestine von Deeb, Samir S., Disteche, Christine, Motulsky, Arno G., Lebo, Roger V., Kan, Yuet W.

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Treatment of hereditary spherocytosis in Peromyscus by radiation and allogeneic bone marrow transplantation von Steinmuller, D, Motulsky, A G

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Homozygous hemoglobin C disease von Thomas, E.D., Motulsky, A.G., Walters, D.H.

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Hemoglobin-Seattle (α2Aβ276Glu): An Unstable Hemoglobin Causing Chronic Hemolytic Anemia von Huehns, E.R, Hecht, F., Yoshida, A., Stamatoyannopoulos, G., Hartman, J., Motulsky, A.G

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Detection of Glucose-6-Phosphate Dehydrogenase Deficient Heterozygotes von STAMATOYANNOPOULOS, G., PAPAYANNOPOULOU, TH, BAKOPOULOS, CHR, MOTULSKY, A.G.

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WERNER'S SYNDROME: CHROMOSOMES, GENES, AND THE AGEING PROCESS von Motulsky, A.G., Schultz, A., Priest, J.

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