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Hemoglobin|June 1, 2005
ATR-16 due to a de novo complex rearrangement of chromosome 16Marta S Gallego, Gabriela Zelaya, Aurora S Feliu, et al.Hemoglobin|June 1, 2005
Two new delta-globin mutations: Hb A2-Ninive [delta133(H11)Val-Ala] and a delta(+)-thalassemia mutation [-31 (A --> G)] in the TATA box of the delta-globin geneHannes Frischknecht, Fabrizio DutlyHemoglobin|August 24, 2005
Hb Oegstgeest [alpha104(G11)Cys-->Ser (alpha1)]. A new hemoglobin variant associated with a mild alpha-thalassemia phenotypeCornelis L Harteveld, Lieke Rozendaal, Nico A Blom, et al.Hemoglobin|August 24, 2005
In vivo action of Vanillin on delay time determined by magnetic relaxationAdolfo Fernández García, Carlos Cabal, Jorge Losada, et al.Hemoglobin|August 24, 2005
Two French Caucasian families with dominant thalassemia-like phenotypes due to hyper unstable hemoglobin variants: Hb Sainte Seve [codon 118 (-T)] and codon 127 [CAG-->TAG (Gln-->stop])Claude Préhu, Serge Pissard, Maha Al-Sheikh, et al.Hemoglobin|August 1, 1993
Black alpha-thalassemia-1: partial characterization of an approximately 80 kb deletion which includes the zeta- and alpha-globin genesT H Huisman, L H Gu, J C Liu, 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|February 1, 1993
DNA polymorphisms associated with Hb D-Los Angeles [beta 121(GH4)Glu-->Gln] in southern ItalyG Fioretti, M De Angioletti, L Pagano, et al.Hemoglobin|January 1, 1980
The organization of the gamma-delta-beta gene complex in normal and thalassemia cellsA Bank, J G Mears, F Ramirez, et al.Hemoglobin|April 10, 2002
A novel beta0-thalassemia mutation at codon 55 (-A) and a rare 17 bp deletion at codons 126-131 in the Indian populationAnita Nadkarni, Takehisa Sakaguchi, Hiroshi Takaku, et al.Pageof 240