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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 spherocytosis
P 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 Benin
C Glele-Kakai, M Garbarz, M C Lecomte, et al.
Blood
|
July 1, 1988
Molecular cloning of the cDNA for human erythrocyte beta-spectrin
J 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 gene
R A Spritz, P Jagadeeswaran, P V Choudary, et al.
The New England Journal of Medicine
|
April 26, 1979
Prenatal diagnosis of classic hemophilia
S 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 anemia
Heather 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 spherocytosis
S W Eber, J M Gonzalez, M L Lux, et al.
Cell
|
October 1, 1980
The structure and evolution of the human beta-globin gene family
A 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 Estimates
B 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 homozygotes
Zhihua Jiang, Hong-Yuan Luo, Shengwen Huang, et al.
Page
of 17
Search research articles
Search
Showing results (161-170 of 170) with videos related to
Sort By:
Page
of 17
You have reached the last page of results.
This site can display upto 170 results.
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 spherocytosis
P 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 Benin
C Glele-Kakai, M Garbarz, M C Lecomte, et al.
Blood
|
July 1, 1988
Molecular cloning of the cDNA for human erythrocyte beta-spectrin
J 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 gene
R A Spritz, P Jagadeeswaran, P V Choudary, et al.
The New England Journal of Medicine
|
April 26, 1979
Prenatal diagnosis of classic hemophilia
S 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 anemia
Heather 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 spherocytosis
S W Eber, J M Gonzalez, M L Lux, et al.
Cell
|
October 1, 1980
The structure and evolution of the human beta-globin gene family
A 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 Estimates
B 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 homozygotes
Zhihua Jiang, Hong-Yuan Luo, Shengwen Huang, et al.
Page
of 17