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British Journal of Haematology|October 1, 1996
Epidemiological studies of spectrin mutations related to hereditary elliptocytosis and spectrin polymorphisms in BeninC Glele-Kakai, M Garbarz, M C Lecomte, et al.
Blood|July 1, 1988
Molecular cloning of the cDNA for human erythrocyte beta-spectrinJ C Winkelmann, T L Leto, P C Watkins, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 1, 1981
Base substitution in an intervening sequence of a beta+-thalassemic human globin geneR A Spritz, P Jagadeeswaran, P V Choudary, et al.
The New England Journal of Medicine|April 26, 1979
Prenatal diagnosis of classic hemophiliaS I Firshein, L W Hoyer, J Lazarchick, et al.
Hemoglobin|October 28, 2014
Hb Youngstown [β101(G3)Glu → Ala; HBB: c.305A > C]: An unstable hemoglobin variant causing severe hemolytic anemiaHeather L Edward, Louis Almero Du Pisani, Walter E Rodriguez-Romero, et al.
Nature Genetics|June 1, 1996
Ankyrin-1 mutations are a major cause of dominant and recessive hereditary spherocytosisS W Eber, J M Gonzalez, M L Lux, et al.
The International Journal of Cardiovascular Imaging|November 9, 2021
The diagnostic accuracy of truncated cardiovascular MR protocols for detecting non-ischemic cardiomyopathiesK Hirschberg, Sz M Braun, O Paul, et al.
Cell|October 1, 1980
The structure and evolution of the human beta-globin gene familyA Efstratiadis, J W Posakony, T Maniatis, et al.
Surveys in Geophysics|December 30, 2024
North Atlantic Heat Transport Convergence Derived from a Regional Energy Budget Using Different Ocean Heat Content EstimatesB Meyssignac, S Fourest, Michael Mayer, et al.
British Journal of Haematology|January 16, 2016
The genetic basis of asymptomatic codon 8 frame-shift (HBB:c25_26delAA) β(0) -thalassaemia homozygotesZhihua Jiang, Hong-Yuan Luo, Shengwen Huang, et al.
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