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Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1975
Demonstration of non-functional beta-globin mRNA in homozygous beta (0) thalassemia
Y W Kan, J P Holland, A M Dozy, et al.
The Journal of Clinical Investigation
|
June 1, 1979
Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes
S H Embury, R V Lebo, A M Dozy, et al.
Blood
|
December 1, 1979
The alpha-globin gene adjacent to the gene for HbQ-alpha 74 Asp replaced by His is deleted, but not that adjacent to the gene for HbG-alpha 30 Glu replaced by Gln; three-fourths of the alpha-globin genes are deleted in HbQ-alpha-thalassemia
L E Lie-Injo, A M Dozy, Y W Kan, et al.
The Journal of Pediatrics
|
February 1, 1978
Prenatal diagnosis of hemoglobin H disease
H M Koenig, T S Vedvick, A M Dozy, et al.
The Journal of Clinical Investigation
|
October 1, 1979
Modification of hemoglobin H disease by sickle trait
K K Matthay, W C Mentzer, A M Dozy, et al.
The Journal of Clinical Investigation
|
December 1, 1980
Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype
S H Embury, J A Miller, A M Dozy, et al.
British Journal of Haematology
|
December 1, 1980
Globin chain synthesis in haemoglobin New York (beta 113 replaced by glutamic acid)
D Todd, V Chan, R G Schneider, et al.
Blood
|
April 1, 1980
Alpha globin gene number: population and restriction endonuclease studies
G Brittenham, B Lozoff, J W Harris, et al.
Blood
|
December 1, 1979
Molecular basis of hemoglobin-H disease in the Mediterranean population
Y W Kan, A M Dozy, G Stamatoyannopoulos, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1980
Triplicated alpha-globin loci in humans
M Goossens, A M Dozy, S H Embury, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 27) with videos related to
Sort By:
Page
of 3
Proceedings of the National Academy of Sciences of the United States of America
|
December 1, 1975
Demonstration of non-functional beta-globin mRNA in homozygous beta (0) thalassemia
Y W Kan, J P Holland, A M Dozy, et al.
The Journal of Clinical Investigation
|
June 1, 1979
Organization of the alpha-globin genes in the Chinese alpha-thalassemia syndromes
S H Embury, R V Lebo, A M Dozy, et al.
Blood
|
December 1, 1979
The alpha-globin gene adjacent to the gene for HbQ-alpha 74 Asp replaced by His is deleted, but not that adjacent to the gene for HbG-alpha 30 Glu replaced by Gln; three-fourths of the alpha-globin genes are deleted in HbQ-alpha-thalassemia
L E Lie-Injo, A M Dozy, Y W Kan, et al.
The Journal of Pediatrics
|
February 1, 1978
Prenatal diagnosis of hemoglobin H disease
H M Koenig, T S Vedvick, A M Dozy, et al.
The Journal of Clinical Investigation
|
October 1, 1979
Modification of hemoglobin H disease by sickle trait
K K Matthay, W C Mentzer, A M Dozy, et al.
The Journal of Clinical Investigation
|
December 1, 1980
Two different molecular organizations account for the single alpha-globin gene of the alpha-thalassemia-2 genotype
S H Embury, J A Miller, A M Dozy, et al.
British Journal of Haematology
|
December 1, 1980
Globin chain synthesis in haemoglobin New York (beta 113 replaced by glutamic acid)
D Todd, V Chan, R G Schneider, et al.
Blood
|
April 1, 1980
Alpha globin gene number: population and restriction endonuclease studies
G Brittenham, B Lozoff, J W Harris, et al.
Blood
|
December 1, 1979
Molecular basis of hemoglobin-H disease in the Mediterranean population
Y W Kan, A M Dozy, G Stamatoyannopoulos, et al.
Proceedings of the National Academy of Sciences of the United States of America
|
January 1, 1980
Triplicated alpha-globin loci in humans
M Goossens, A M Dozy, S H Embury, et al.
Page
of 3