Cosegregation of elastin-associated microfibrillar abnormalities with the Marfan phenotype in families von GODFREY, M, MENASHE, V, WELEBER, R. G, KOLER, R. D, BIGLEY, R. H, LOVRIEN, E, ZONANA, J, HOLLISTER, D. W

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Citrullinemia: enzymatic evidence for genetic heterogeneity von Kennaway, N G, Harwood, P J, Ramberg, D A, Koler, R D, Buist, N R

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Erythrocytosis Secondary to Increased Oxygen Affinity of a Mutant Hemoglobin, Hemoglobin Kempsey von Reed, Con S., Hampson, Roger, Gordon, Susan, Jones, Richard T., Novy, Miles J., Brimhall, Bernadine, Edwards, Miles J., Koler, Robert D.

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Isolation and functional characterization of hemoglobin Casper. β106(G8)Leu → Pro von Wajcman, Henri, Gacon, Gerard, Labie, Dominique, Koler, Robert D, Jones, Richard T

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Red blood cell survival in patients with aortic valvular disease and ball-valve prostheses von Brodeur, M T, Sutherland, D W, Koler, R D, Starr, A, Kimsey, J A, Griswold, H E

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Ontogeny of Soluble and Mitochondrial Tyrosine Aminotransferases von Koler, Robert D., Vanbellinghen, Patricia J., Fellman, J. H., Jones, Richard T., Behrman, Richard E.

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Soluble and mitochondrial forms of tyrosine aminotransferase. Relation to human tyrosinemia von Fellman, Jacob H, Vanbellinghen, Patricia J, Jones, Richard Theodore, Koler, Robert D

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Pregnancy In Carriers of High-Affinity Hemoglobins von Charache, Samuel, Catalano, Patrick, Burns, Stanley, Jones, Richard T., Koler, Robert D., Rutstein, Richard, Williams, Robert R., Hathaway, with the technical assistance of Patricia J.

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Therapy‐related preleukemic syndrome von Anderson, Robert L., Bagby, GROVER, C., Richert‐Boe, Kathryn, Magenis, R. Ellen, Koler, Robert D.

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Obituary for Dr. Edwin E. Osgood, M.D von KOLER, ROBERT D.

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Catalog of Genetic Variations: Mendelian Inheritance in Man . Catalogs of Autosomal Dominant, Autosomal Recessive, and X-Linked Phenotypes. Victor A. McKusick. Johns Hopkins Press,... von Koler, Robert D.

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Synthesis of erythrocyte-specific proteins in cultured friend leukemia cells von Kabat, David, Sherton, Corinne C., Evans, Leonard H., Bigley, Robert, Koler, Robert D.

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HUMAN HEMOGLOBIN MUTATIONS von Koler, Robert D.

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Hemoglobin Yakima: I. Clinical and Biochemical Studies von Jones, Richard T., Osgood, Edwin E., Brimhall, Bernadine, Koler, Robert D.

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EDWIN E. OSGOOD, M.D von Koler, Robert D.

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Catalog of Genetic Variations von Koler, Robert D.

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Gene Dosage: Evidence for Assignment of Erythrocyte Acid Phosphatase Locus to Chromosome 2 von Magenis, R. Ellen, Koler, Robert D., Lovrien, Everett, Bigley, Robert H., DuVal, Michael C., Overton, Kathleen M.

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Hemoglobin Linkoping [β36 (C2) Pro→Thr] in a Large Finnish Family from Astoria, Oregon, USA von Jones, Richard T., Head, Charlotte, Shih, Marjorie F. C., Shih, Daniel T. B., Dana, Bruce, Jones, Marilyn B., Koler, Robert D.

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Hemoglobin Chico [β66(E10)Lys→Thr]: A New Variant with Decreased Oxygen Affinity von Shih, Daniel T-b., Jones, Richard T., Shih, Marjorie F-C., Jones, Marilyn B., Koler, Robert D., Howard, John

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Hemoglobin Yakima: I. Clinical and Biochemical Studies von Jones, Richard T., Osgood, Edwin E., Brimhall, Bernadine, Koler, Robert D.

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