Short Tandem-Repeat Polymorphism/ Alu Haplotype Variation at the PLAT Locus: Implications for Modern Human Origins von Tishkoff, S.A., Pakstis, A.J., Stoneking, M., Kidd, J.R., Destro-Bisol, G., Sanjantila, A., Lu, R.-b., Deinard, A.S., Sirugo, G., Jenkins, T., Kidd, K.K., Clark, A.G.

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A Global Haplotype Analysis of the Myotonic Dystrophy Locus: Implications for the Evolution of Modern Humans and for the Origin of Myotonic Dystrophy Mutations von Tishkoff, S.A., Goldman, A., Calafell, F., Speed, W.C., Deinard, A.S., Bonne-Tamir, B., Kidd, J.R., Pakstis, A.J., Jenkins, T., Kidd, K.K.

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A dinucleotide repeat polymorphism at the HOX2B locus von Deinard, A.S., Ruano, G., Kidd, K.K.

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Cognitive deficits in iron-deficient and iron-deficient anemic children von Deinard, Amos S., List, Anne, Lindgren, Bruce, Hunt, Jane V., Chang, Pi-Nian

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Screening for iron deficiency with the erythrocyte protoporphyrin test [Serum ferritin] von Yip, R, Schwartz, S, Deinard, A.S

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RUBELLA-ANTIBODY TITRES IN RHEUMATOID ARTHRITIS von Deinard, A.S., Bilka, P.J., Venters, H.D., Herrmann, K.L., Page, A.R.

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