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British Journal of Haematology|October 1, 1994
The differences in quantities of alpha 2- and alpha 1-globin gene variants in heterozygotesT P Molchanova, D D Pobedimskaya, T H HuismanAmerican Journal of Hematology|November 1, 1994
Compound heterozygosity for two alpha-globin gene defects, Hb Taybe (alpha 1; 38 or 39 minus Thr) and a poly A mutation (alpha 2; AATAAA-->AATAAG), results in a severe hemolytic anemiaD D Pobedimskaya, T P Molchanova, S Streichman, et al.American Journal of Hematology|April 1, 1994
Two different mutations in codon 68 are observed in Hb G-Philadelphia heterozygotesT P Molchanova, D D Pobedimskaya, Z Ye, et al.Hemoglobin|December 1, 1993
Hb Sinai-Baltimore or alpha 2 beta (2)18(A15)Val->Gly, a silent, mildly unstable beta chain variant detected by isoelectrofocusing and high performance liquid chromatographyD D Pobedimskaya, T P Molchanova, R Amernick, et al.Hemoglobin|September 1, 1994
Hb Fannin-Lubbock in five Spanish families is characterized by two mutations: beta 111 GTC-->CTC (Val-->Leu) and beta 119 GGC-->GAC (Gly-->Asp)W B Qin, D D Pobedimskaya, T P Molchanova, et al.Hemoglobin|June 1, 1993
Hb Alesha or alpha 2 beta (2)67(E11)Val-->Met: a new unstable hemoglobin variant identified through sequencing of amplified DNAT P Molchanova, Postnikov YuV, D D Pobedimskaya, et al.American Journal of Hematology|January 1, 1994
Quantities of alpha Q chain variants in heterozygotes with and without a concomitant beta-thalassemia traitW B Qin, E Baysal, K F Wong, et al.American Journal of Hematology|August 1, 1994
Beta-thalassemia alleles and unstable hemoglobin types among Russian pediatric patientsM A Cürük, T P Molchanova, Postnikov YuV, et al.Hemoglobin|May 1, 1995
Hb Bibba or alpha 2 136(H19)Leu-->Pro beta 2 in a Caucasian family from AlabamaJ T Prchal, B Adler, J B Wilson, et al.Pageof 1