Hb S, Hb G-Philadelphia and alpha-thalassemia-2 in a Black family von Felice, A E, Mayson, S M, Webber, B B, Miller, A, Gravely, M E, Huisman, T H

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Delta beta-thalassemia in a Mexican family: clinical differences among homozygotes von Reyes, G R, Piña-Camara, A, Felice, A E, Gravely, M E, Huisman, T H

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Oxygen equilibrium analyses of isolated hemoglobins A2, Lepore-Washington and P-Nilotic von Raybourne, S.R., Stallings, M.B., Gravely, M.E., Huisman, T.H.J.

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Hemoglobinopathies Observed in the Population of the Southeastern United States (SE-USA) von Huisman, T. H. J., Abraham, B. L., Harris, H. F., Gravely, M. E., Henson, J., Williams, D., Wilson, J. B., Miller, A., Mayson, S., Wrightstone, R. N., Moss, E., Joseph, B., Walker, L., Brisco, J., Brisco, L.

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A note on the inheritance of the hereditary persistence of fetal haemoglobin and the delta-chain variant Hb-A2 von Huisman, T H, Gravely, M E, Sox, R

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Quantitation of three types of gamma chain of HbF by high pressure liquid chromatography; application of this method to the HbF of patients with sickle cell anemia or the S-HPFH co... von Huisman, TH, Altay, C, Webber, B, Reese, AL, Gravely, ME, Okonjo, K, Wilson, JB

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The Gamma Chain Heterogeneity of Fetal Hemoglobin in Black β-Thalassemia and HPFH Heterozygotes von Huisman, T.H.J., Gravely, M.E., Webber, B., Okonjo, K., Henson, J., Reese, A.L.

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alpha-thalassemia-2 and the variability of hematological values in children with sickle cell anemia von Altay, C, Gravely, M E, Joseph, B R, Williams, D F

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THE RATIO OF Gγ AND Aγ CHAINS OF THE HEMOGLOBIN F SYNTHESIZED BY BFU-E-DERIVED COLONIES FROM BLOOD OF SUBJECTS WITH β+ THALASSEMIA AND RELATED HEMOGLOBINOPATHIES von Huisman, T. H. J., Efremov, G. D., Reese, A. L., Howard, J. S., Gravely, M. E., Wilson, J. B.

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The association of sickle cell anemia with heterozygous and homozygous α‐thalassemia‐2: In vitro HB chain synthesis von Felice, A. E., Webber, B., Miller, A., Mayson, S. M., Harris, H. F., Henson, J. B., Gravely, M. E., Huisman, T. H. J.

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The gamma chain heterogeneity of fetal hemoglobin in black beta- thalassemia and HPFH heterozygotes von Huisman, TH, Gravely, ME, Webber, B, Okonjo, K, Henson, J, Reese, AL

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The synthesis of the Gγ and Aγ chains of human fetal hemoglobin in erythroid colonies cultured from peripheral blood BFUe's of normal adults and newborn and of subjects with an Aγ... von Huisman, T. H. J., Reese, A. L., Gravely, M. E., Harris, H., Wilson, J. B.

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Adult and fetal hemoglobin production in erythroid colonies from subjects with beta-thalassemia or with hereditary persistance of fetal hemoglobin (HPFH) von Huisman, T H, Reese, A L, Gravely, M E, Wilson, J B, Webber, B, Felice, A E

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The synthesis of fetal hemoglobin types in red blood cells and in BFU-E derived colonies from peripheral blood of patients with sickle cell anemia, beta+ - and delta beta-thalassem... von Huisman, T H, Efremov, G D, Reese, A L, Howard, J S, Gravely, M E, Harris, H F, Wilson, J B

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Quantitation of Three Types of γ Chain of HbF by High Pressure Liquid Chromatography; Application of This Method to the HbF of Patients With Sickle Cell Anemia or the S-HPFH Condit... von Huisman, T.H.J., Altay, C., Webber, B., Reese, A.L., Gravely, M.E., Okonjo, K., Wilson, J.B.

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Interaction of the β chain variant hemoglobin leslie and the α chain variant hemoglobin montgomery in a black female von Huisman, T. H. J., Gravely, M. E., Wilson, J. B., Webber, B., Felice, A. E., Miller, A.

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Adult and Fetal Hemoglobin Production in Erythroid Colonies from Subjects with β-Thalassemia or with Hereditary Persistence of Fetal Hemoglobin (HPFH) von Huisman, T. H. J., Reese, A. L., Gravely, M. E., Wilson, J. B., Webber, B., Felice, A. E.

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Hb Leslie, an unstable hemoglobin due to deletion of glutaminyl residue beta 131 (H9) occurring in association with beta0-thalassemia, HbC, and HbS von Lutcher, C L, Wilson, J B, Gravely, M E, Stevens, P D, Chen, C J, Lindeman, J G, Wong, S C, Miller, A, Gottleib, M, Huisman, T H

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Hb Nottingham (α;2β;2 (FG5) 98 VAL→GLY) in a Caucasian Male: Clinical and Biosynthetic Studies von Orringer, E. P., Felice, A., Reese, A., Wilson, J. B., Lam, H., Gravely, M. E., Huisman, T. H. J.

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Hb Suresnes or alpha2 141(HC3) ArgyieldHis beta2 in a black family von Gravely, M E, Harris, H F, Stallings, M, Lam, H, Wilson, J B, Huisman, T H

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