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B G Forget

Showing results (181-190 of 192) with videos related to

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American Journal of Hematology|March 1, 1997
Amino-acid substitution in alpha-spectrin commonly coinherited with nondominant hereditary spherocytosisW T Tse, P G Gallagher, P B Jenkins, et al.
Annals of the New York Academy of Sciences|January 1, 1980
Heterogeneity of messenger RNA defects in the thalassemia syndromesE J Benz, J Glass, G A Tsistrakis, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1980
Embryonic-fetal erythroid characteristics of a human leukemic cell lineE J Benz, M J Murnane, B L Tonkonow, et al.
The Journal of Clinical Investigation|January 15, 1996
A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosisP B Jenkins, G K Abou-Alfa, D Dhermy, et al.
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.
Annals of the New York Academy of Sciences|January 1, 1974
Globin messenger RNA in the thalassemia syndromesB G Forget, D Baltimore, E J Benz, 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.
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.
Pageof 20

Showing results (181-190 of 192) with videos related to

Sort By:
Pageof 20
American Journal of Hematology|March 1, 1997
Amino-acid substitution in alpha-spectrin commonly coinherited with nondominant hereditary spherocytosisW T Tse, P G Gallagher, P B Jenkins, et al.
Annals of the New York Academy of Sciences|January 1, 1980
Heterogeneity of messenger RNA defects in the thalassemia syndromesE J Benz, J Glass, G A Tsistrakis, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1980
Embryonic-fetal erythroid characteristics of a human leukemic cell lineE J Benz, M J Murnane, B L Tonkonow, et al.
The Journal of Clinical Investigation|January 15, 1996
A nonsense mutation in the erythrocyte band 3 gene associated with decreased mRNA accumulation in a kindred with dominant hereditary spherocytosisP B Jenkins, G K Abou-Alfa, D Dhermy, et al.
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.
Annals of the New York Academy of Sciences|January 1, 1974
Globin messenger RNA in the thalassemia syndromesB G Forget, D Baltimore, E J Benz, 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.
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.
Pageof 20