Observations on the levels of Hb A2 in patients with different β-thalassemia mutations and a δ chain variant von CODRINGTON, J. F, LI, H.-W, KUTLAR, F, GU, L.-H, RAMACHANDRAN, M, HUISMAN, T. H. J

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Types of Thalassemia Among Patients Attending a Large University Clinic in Kuala Lumpur, Malaysia von George, E., Li, H-J., Fei, Y-J., Reese, A. L., Baysal, E., Cepreganova, B., Wilson, J. B., Gu, L-H., Nechtman, J. F., Stoming, T. A., Liu, J-C., Codrington, J. F., Huisman, T. H. J.

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Hemoglobin Birmingham and Hemoglobin Galicia: Two Unstable β Chain Variants Characterized by Small Deletions and Insertions von Wilson, J.B., Webber, B.B., Hu, H., Kutlar, A., Kutlar, F., Codrington, J.F., Prchal, J.T., Hall, K.M., Pablos, J.M. de, Rodriguez, I., Huisman, T.H.J.

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The Usefulness of Sequence Analysis of Amplified DNA for the Identification of δ Chain Variants von Li, H-W., Codrington, J. F., Schiliro, G., Wadsworth, L. D., Beris, Ph, Adekile, A., Huisman, T. H.J.

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Hemoglobin Birmingham and hemoglobin Galicia: two unstable beta chain variants characterized by small deletions and insertions von Wilson, JB, Webber, BB, Hu, H, Kutlar, A, Kutlar, F, Codrington, JF, Prchal, JT, Hall, KM, de Pablos, JM, Rodriguez, I

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Hb Chad or alpha 223(B4)Glu----Lys beta 2 observed in members of a Surinam family in association with alpha-thalassemia-2 and with Hb S von Codrington, J F, Codrington, F A, Wisse, J H, Wilson, J B, Webber, B B, Wong, S C, Huisman, T H

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