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Hemoglobin|August 7, 2009
Molecular heterogeneity of beta-thalassemia alleles in Spain and its importance in the diagnosis and prevention of beta-thalassemia major and sickle cell disordersMaria del Mar Mañú Pereira, Anna Cabot Dalmau, Joan-Lluis Vives CorronsHemoglobin|August 7, 2009
Alpha-thalassemia mutations in Gilan Province, North IranValeh Hadavi, Maryam Jafroodi, Nima Hafezi-Nejad, et al.Hemoglobin|March 23, 2011
Hb A2' (Hb B2) in the Omani population and diagnostic significanceShahina Daar, Shoaib Al Zadjali, David Gravell, et al.Hemoglobin|March 23, 2011
Detection of Hb Setif in north Iran and the question of its origin: Iranian or multiethnic?Mohammad Reza Mahdavi, Mehran Karimi, Majid Yavarian, et al.Hemoglobin|March 11, 1998
DNA sequence analysis proves Hb M-Milwaukee-2 is due to beta-globin gene codon 92 (CAC-->TAC), the presumed mutation of Hb M-Hyde Park and Hb M-AkitaP J Hutt, A V Pisciotta, V F Fairbanks, et al.Hemoglobin|March 11, 1998
Hb Godavari [alpha 95(G2)Pro-->Thr]: a neutral amino acid substitution in the alpha 1 beta 2 interface that modifies the electrophoretic mobility of hemoglobinH Wajcman, J Kister, J Riou, et al.Hemoglobin|March 11, 1998
Hb Peterborough [beta 111(G13)Val-->Phe] in Japan; rapid identification by ESI/MS using proteolytic digests of oxidized globinT Nakanishi, A Miyazaki, M Kishikawa, et al.Hemoglobin|January 1, 1980
Do amino acids reverse the sickling of erythrocytes containing hemoglobin S?K Shirahama, S Kubota, J T YangHemoglobin|January 1, 1980
A new hemoblogin variant in hungary: Hb Savaria - alpha 49 (CE7) Ser replace by ArgJ G Szelényi, M Horányi, J Földi, et al.Hemoglobin|October 10, 1997
Prenatal diagnosis of beta-thalassemia among Indians using denaturing gradient gel electrophoresisA C Gorakshakar, C P Lulla, A H Nadkarni, et al.Pageof 240