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The New England Journal of Medicine
|
September 1, 1994
Therapy for beta-thalassemia--a paradigm for the treatment of genetic disorders
G J Dover, D Valle
Progress in Clinical and Biological Research
|
January 1, 1987
The effect of increased fetal hemoglobin production on the frequency of vaso-occlusive crisis in sickle cell disease
G J Dover, S Charache
Progress in Clinical and Biological Research
|
January 1, 1984
The effects of variable doses of 5-azacytidine on fetal hemoglobin production in sickle cell anemia
G J Dover, S H Charache
Current Opinion in Pediatrics
|
February 15, 2001
Sickle cell disease: no longer a single gene disorder
D H Chui, G J Dover
Blood
|
December 1, 1980
Quantitation of hemoglobins within individual red cells: asynchronous biosynthesis of fetal and adult hemoglobin during erythroid maturation in normal subjects
G J Dover, S H Boyer
Progress in Clinical and Biological Research
|
January 1, 1981
Hemoglobin determinations in single cells: Comparison of different techniques
G J Dover, S H Boyer
Blood
|
April 1, 1987
Fetal hemoglobin-containing cells have the same mean corpuscular hemoglobin as cells without fetal hemoglobin: a reciprocal relationship between gamma- and beta-globin gene expression in normal subjects and in those with high fetal hemoglobin production
G J Dover, S H Boyer
Texas Reports on Biology and Medicine
|
January 1, 1980
The cellular distribution of fetal hemoglobin: normal adults and hemoglobinopathies
G J Dover, S H Boyer
Blood
|
July 1, 1994
Induction of fetal hemoglobin production in subjects with sickle cell anemia by oral sodium phenylbutyrate
G J Dover, S Brusilow, S Charache
Blood
|
June 1, 1983
Fetal hemoglobin production in cultures of primitive and mature human erythroid progenitors: differentiation affects the quantity of fetal hemoglobin produced per fetal-hemoglobin-containing cell
G J Dover, T Chan, F Sieber
Page
of 8
Search research articles
Search
Showing results (11-20 of 80) with videos related to
Sort By:
Page
of 8
The New England Journal of Medicine
|
September 1, 1994
Therapy for beta-thalassemia--a paradigm for the treatment of genetic disorders
G J Dover, D Valle
Progress in Clinical and Biological Research
|
January 1, 1987
The effect of increased fetal hemoglobin production on the frequency of vaso-occlusive crisis in sickle cell disease
G J Dover, S Charache
Progress in Clinical and Biological Research
|
January 1, 1984
The effects of variable doses of 5-azacytidine on fetal hemoglobin production in sickle cell anemia
G J Dover, S H Charache
Current Opinion in Pediatrics
|
February 15, 2001
Sickle cell disease: no longer a single gene disorder
D H Chui, G J Dover
Blood
|
December 1, 1980
Quantitation of hemoglobins within individual red cells: asynchronous biosynthesis of fetal and adult hemoglobin during erythroid maturation in normal subjects
G J Dover, S H Boyer
Progress in Clinical and Biological Research
|
January 1, 1981
Hemoglobin determinations in single cells: Comparison of different techniques
G J Dover, S H Boyer
Blood
|
April 1, 1987
Fetal hemoglobin-containing cells have the same mean corpuscular hemoglobin as cells without fetal hemoglobin: a reciprocal relationship between gamma- and beta-globin gene expression in normal subjects and in those with high fetal hemoglobin production
G J Dover, S H Boyer
Texas Reports on Biology and Medicine
|
January 1, 1980
The cellular distribution of fetal hemoglobin: normal adults and hemoglobinopathies
G J Dover, S H Boyer
Blood
|
July 1, 1994
Induction of fetal hemoglobin production in subjects with sickle cell anemia by oral sodium phenylbutyrate
G J Dover, S Brusilow, S Charache
Blood
|
June 1, 1983
Fetal hemoglobin production in cultures of primitive and mature human erythroid progenitors: differentiation affects the quantity of fetal hemoglobin produced per fetal-hemoglobin-containing cell
G J Dover, T Chan, F Sieber
Page
of 8