Variability in the fetal hemoglobin level of the normal adult von Leonova, Julia Ye, Kazanetz, Elena G., Smetanina, Natalia S., Adekile, Adekunle D., Efremov, Georgi D., Huisman, Titus H.J.

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Co-inheritance of Hb D-Punjab (codon 121; GAA-->CAA) and beta (0) -thalassemia (IVS-II-1;G-->A) von Adekile, A D, Kazanetz, E G, Leonova, J Y, Marouf, R, Khmis, A, Huisman, T H

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Co-inheritance of Hb D-PUNJAB (CODON 121; GAA→CAA) and β0-thalassemia (IVS-II-1; G→A) von ADEKILE, A. D, KAZANETZ, E. G, LEONOVA, J. YE, MAROUF, R, KHMIS, A, HUISMAN, T. H. J

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HB Mizuho or α2β268(E12)LEU→PRO in a Young Dutch Boy von Harthoorn-lasthuizen, E. J., Nabben, F. A. E., Kazanetz, E. G., Gu, L.-H., Molchanova, T. P., Huisman, T. H. J.

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HB Mizuho or alpha 2 beta 2 68(E12)Leu-->Pro in a young Dutch boy von Harthoorn-Lasthuizen, E J, Nabben, F A, Kazanetz, E G, Gu, L H, Molchanova, T P, Huisman, T H

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HB Bibba OR α2136(H19)LEU→PROβ2 in a Caucasian Family from Alabama von Prchal, J. T., Adler, B., Wilson, J. B., Baysal, E., Qin, W.-B., Molchanova, T. P., Pobedimskaya, D. D., Kazanetz, E. G., Huisman, T. H. J.

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Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2 in a Caucasian family from Alabama von Prchal, J T, Adler, B, Wilson, J B, Baysal, E, Qin, W B, Molchanova, T P, Pobedimskaya, D D, Kazanetz, E G, Huisman, T H

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Hb Nunobiki or alpha 2 141 (HC3)Arg-->Cys beta 2 in a Belgian female results from a CGT-->TGT mutation in the alpha 2-globin gene von Kazanetz, E G, Leonova, J Y, Huisman, T H, van der Dijs, F P, Smit, J W

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β-Thalassemia Intermedia in An Indian Female h the Hb Hofu [β126(H4)Val→Glu]-(β°-Thalassemia [Codons 8/9 (+G)] Combination von Pande, P. L., Prakash, S., Tiwary, R. S., Kazanetz, E. G., Leonova, J. Ye, Huisman, T. H.J.

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Hb Nunoi or α2141(Hc3)Arg → Cysβ2 In A Belgian Female Results From A Cgt → T gt Mutation In The α2-Globin Gene von Kazanetz, E. G., Leonova, J. Ye, Huisman, T. H.J., van der Dijs, F. P.L., Smit, J. W.

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Hb Nunoi or α 2 141(Hc3)Arg → Cysβ 2 In A Belgian Female Results From A Cgt → T gt Mutation In The α2-Globin Gene von Kazanetz, E. G., Leonova, J. Ye, Huisman, T. H.J., van der Dijs, F. P.L., Smit, J. W.

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Beta-thalassemia intermedia in an Indian female with the Hb Hofu [beta 126(H4)Val-->Glu]-beta zero-thalassemia [codons 8/9 (+G)] combination von Pande, P L, Prakash, S, Tiwary, R S, Kazanetz, E G, Leonova J, Y e, Huisman, T H

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β-thalassemia intermedia in an Indian female with the Hb Hofu [β126(H4)Val→Glu]-β0-thalassemia [Codons 8/9 (+G)] combination von PANDE, P. L, PRAKASH, S, TIWARY, R. S, KAZANETZ, E. G, LEONOVA, J. Y, HUISMAN, T. H. J

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Hb ananosa or α2111(G18)Ala → Valβ (α2 Mutation) and Hb mulhacen or α2123(H6)Ala → Serβ2 (αl Mutation) are two silent stable variants detected by sequencing of amplified dna... von Kazanetz, E. G., Leonova, J. Ye, Wilson, J. B., McMillan, S. K., Walbrecht, M., de Pablos Gallego, J. Mi, Huisman, T. H. J.

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Hb Anamosa or α2111(G18)Ala→Valβ2 (α2 mutation) and Hb Mulhacen or α2123(H6)Ala→Serβ2 (α1 mutation) are two silent, stable variants detected by sequencing of amplified DNA... von KAZANETZ, E. G, LEONOVA, J. YE, WILSON, J. B, MCMILLAN, S. K, WALBRECHT, M, DE PABLOS GALLEGO, J. M, HUISMAN, T. H. J

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Hb ananosa or α2111(G18)Ala → Valβ (α2 Mutation) and Hb mulhacen or α2123(H6)Ala → Serβ2 (αl Mutation) are two silent stable variants detected by sequencing of amplified dna... von Kazanetz, E. G., Leonova, J. Ye, Wilson, J. B., McMillan, S. K., Walbrecht, M., Gallego, J. Mi. de Pablos, Huisman, T. H. J.

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Hb ananosa or α 2 111(G18)Ala → Valβ (α2 Mutation) and Hb mulhacen or α 2 123(H6)Ala → Serβ 2 (αl Mutation) are two silent stable variants detected by sequencing of amplified dna... von Kazanetz, E. G., Leonova, J. Ye, Wilson, J. B., McMillan, S. K., Walbrecht, M., de Pablos Gallego, J. Mi, Huisman, T. H. J.

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Hb Anamosa or alpha 2(111)(G18)Ala-->Val beta 2 (alpha 2 mutation) and Hb Mulhacen or alpha 2(123)(H6)Ala-->Ser beta 2 (alpha 1 mutation) are two silent, stable variants detected b... von Kazanetz, E G, Leonova, J Y, Wilson, J B, McMillan, S K, Walbrecht, M, de Pablos Gallego, J M, Huisman, T H

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HB Alesha or α2 β267(E11)VAL →MET: A New Unstable Hemoglobin Variant Identified Through Sequencing of, Amplified DNA von Molchanova, T. P., Postnikov, Yu. V., Pobedimskaya, D. D., Smetanina, N. S., Moschan, A. A., Kazanetz, E. G., Tokarev, Yu. N., Huisman, T. H. J.

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Hb Alesha or alpha 2 beta (2)67(E11)Val-->Met: a new unstable hemoglobin variant identified through sequencing of amplified DNA von Molchanova, T P, Postnikov YuV, Pobedimskaya, D D, Smetanina, N S, Moschan, A A, Kazanetz, E G, Tokarev YuN, Huisman, T H

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