β-Thalassemia in Southwestern Iran von Merat, A., Haghshenas, M., Pour, Z. Mostafavi, Plonczynski, M. W., Harrell, A. N., Coleman, M. B., Steinberg, M. H.

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β-Thalassemia Intermedia with Exceptionally High Hemoglobin A2: Relationship to Mutations in the β-Gene Promoter von Coleman, Mary B., Adams, Junius G., Plonczynski, Maria W., Harrell, Audrey H., Walker, Alice M., Fairbanks, Virgil, Steinberg, Martin H.

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The -87 (C→A) β+-Thalassemia Mutation in a Black Family von Coleman, M. B., Steinberg, M. H., Harrell, A. H., Plonczynski, M. W., Walker, A. M., Adams, J. G.

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HB San Diego [β109(G11)VAL→MET] in an Iranian: Further Evidence for a Mutational Hot Spot at Position 109 of the β-Globin Gene von Coleman, M. B., Adams, J. G., Walker, A. M., Plonczynski, M. W., Harrell, A. H., Kark, J. A., Schechter, G. P.

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Interleukin-8 Synthesis, Regulation, and Steroidogenic Role in H295R Human Adrenocortical Cells von Romero, Damian G, Vergara, Gaston R, Zhu, Zheng, Covington, Gina S, Plonczynski, Maria W, Yanes, Licy L, Gomez-Sanchez, Elise P, Gomez-Sanchez, Celso E

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GγAγ(β+) hereditary persistence of fetal hemoglobin: The Gγ – 158 C → T mutation in cis to the − 175 T → C mutation of the Aγ‐globin gene results in increased Gγ‐globin synthesis... von Coleman, M. B., Adams, J. G., Steinberg, M. H., Plonczynski, M. W., Harrell, A. H., Castro, O., Winter, W. P.

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GγAγ(β+) hereditary persistence of fetal hemoglobin : the Gγ-158C→T mutation in cis to the -175T→C mutation of the Aγ-globin gene results in increased Gγ-globin synthesis von COLEMAN, M. B, ADAMS, J. G, STEINBERG, M. H, PLONCZYNSKI, M. W, HARRELL, A. H, CASTRO, O, WINTER, W. P

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BETA-THALASSEMIA INTERMEDIA WITH EXCEPTIONALLY HIGH HEMOGLOBIN-A(2) - RELATIONSHIP TO MUTATIONS IN THE BETA-GENE PROMOTER von COLEMAN, MB, ADAMS, JG, PLONCZYNSKI, MW, HARRELL, AH, WALKER, AM, FAIRBANKS, STEINBERG, MH

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Genetic studies suggest a multicentric origin for Hb G-coushatta [β22(B4)Glu→Ala] von Li, J., Wilson, D., Plonczynski, M., Harrell, A., Cook, C. B., Scheer, W. D., Zeng, Y-T., Coleman, M. B., Steinberg, M. H.

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