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Hemoglobin|May 22, 2019
A Krüppel-Like Factor 1 Gene Mutation Ameliorates the Severity of β-Thalassemia: A Case ReportXing-Mei Xie, Ying-Na Liu, Jian Li, et al.Hemoglobin|October 10, 1997
Analysis of mRNA from red cells of patients with thalassemia and hemoglobin variantsN S Smetanina, T P Molchanova, T H HuismanHemoglobin|March 11, 1998
Hb Tak confirmed by DNA analysis: not expressed as thalassemia in a Hb Tak/Hb E compound heterozygoteJ D Hoyer, M J Wick, S N Thibodeau, et al.Hemoglobin|May 12, 1998
HB Les Andelys [alpha83(F4)LEU-->PRO]: a new moderately unstable variantH Wajcman, D Promé, C Préhu, et al.Hemoglobin|May 12, 1998
Molecular basis of beta-thalassemia in the MaldivesH Furuumi, N Firdous, T Inoue, et al.Hemoglobin|January 1, 1980
Hemoglobin takamatsu (beta 120 (GH 3) Lys leads to Gln): a new abnormal hemoglobin detected in three unrelated families in the takamatsu area of shikokuI Iuchi, K Hidaka, T Harano, et al.Hemoglobin|January 1, 1984
Asymmetric hybrids formed with hemoglobin British Columbia (alpha 2 beta 2101Glu----Lys)R A StinsonHemoglobin|January 1, 1982
Construction of human gene libraries from small amounts of peripheral blood: analysis of beta-like globin genesM Poncz, D Solowiejczyk, B Harpel, et al.Hemoglobin|January 1, 1981
Heterozygosity and homozygosity for the high oxygen affinity hemoglobin Tarrant or alpha 126 (H9) Asp replaced by Asn in two Mexican familiesB Ibarra, G Vaca, J M Cantú, et al.Pageof 240