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Hemoglobin|May 1, 1995
Hb Hakkari or alpha 2 beta 2 31(B13)Leu-->Arg, a severely unstable hemoglobin variant associated with numerous intra-erythroblastic inclusions and erythroid hyperplasia of the bone marrowA Gürgey, C Altay, L H Gu, et al.Hemoglobin|March 1, 1997
Selective precipitation of human hemoglobin by organic solvents and metal cationsF Frantzen, K Grimsrud, D E Heggli, et al.Hemoglobin|February 1, 1996
Modulation of the phenotypic diversity of sickle cell anemiaM H SteinbergHemoglobin|February 1, 1996
HB Hinwil or beta 38(C4)Thr-->Asn: a new beta chain variant detected in a Swiss familyH Frischknecht, M Ventruto, D Hess, et al.Hemoglobin|February 1, 1996
beta S haplotypes, alpha-globin gene status, and hematological data of sickle cell disease patients in Guadeloupe (F.W.I.)L Kéclard, V Ollendorf, C Berchel, et al.Hemoglobin|October 1, 1993
Hb Val de Marne [alpha 133(H16)Ser-->Arg]: a new hemoglobin variant with moderate increase in oxygen affinityH Wajcman, J Kister, A M'Rad, et al.Hemoglobin|January 1, 1995
The sickle cell painful crisis in adults: phases and objective signsS K BallasHemoglobin|November 9, 2016
Novel Mutation of the Translation Initiation Codon of the α1-Globin Gene (ATG>AAG or HBA1:c.2T>A)John S Waye, Barry Eng, Meredith Hanna, et al.Hemoglobin|April 1, 2017
Hb Alesha [β67(E11)Val→Met (GTG>ATG); HBB: c.202G > A] Found in a Chinese GirlHua Jiang, Jin-Mei Yan, Jian-Ying Zhou, et al.Pageof 240