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Human Heredity
|
January 1, 1982
Glucose-6-phosphate dehydrogenase and hemoglobin variants in Kel Kummer Tuareg and related groups. Indirect evidence for alpha-thalassemia trait
C Junien, A Chaventré, Y Fofana, et al.
Acta Haematologica
|
January 1, 1976
Congenital enzymopenic methaemoglobinaemia. Clinical and biochemical study of a family with three homozygotes
A Mast, R Milo, C Junien, et al.
Human Genetics
|
January 1, 1983
Four new haplotypes observed in Algerian beta-thalassemia patients
C Beldjord, C Lapouméroulie, M L Baird, et al.
Gene
|
June 19, 1998
Diversity of sequence haplotypes associated with beta-thalassaemia mutations in Algeria: implications for their origin
P Perrin, R Bouhassa, L Mselli, et al.
American Journal of Human Genetics
|
July 1, 1989
Nucleotide variations in the 3' A gamma enhancer region are linked to beta-gene cluster haplotypes and are unrelated to fetal hemoglobin expression
A Ragusa, M Lombardo, E Bouhassira, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Sequence variations in the 3' A gamma enhancer are silent polymorphisms
A Ragusa, M Lombardo, T Lombardo, et al.
Human Genetics
|
June 1, 1993
Inter-ethnic polymorphism of the beta-globin gene locus control region (LCR) in sickle-cell anemia patients
B Périchon, A Ragusa, C Lapouméroulie, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 1983
Influence of thyroid status on hemoglobin A2 expression
J M Kuhn, M Rieu, J Rochette, et al.
Human Genetics
|
January 1, 1984
alpha-Thalassemia among sickle cell anemia patients in various African populations
J Pagnier, O Dunda-Belkhodja, I Zohoun, et al.
American Journal of Hematology
|
July 1, 1991
Preliminary report on the use of desferrioxamine in the treatment of Plasmodium falciparum malaria
O Traore, P Carnevale, L Kaptue-Noche, et al.
Page
of 22
Search research articles
Search
Showing results (171-180 of 212) with videos related to
Sort By:
Page
of 22
Human Heredity
|
January 1, 1982
Glucose-6-phosphate dehydrogenase and hemoglobin variants in Kel Kummer Tuareg and related groups. Indirect evidence for alpha-thalassemia trait
C Junien, A Chaventré, Y Fofana, et al.
Acta Haematologica
|
January 1, 1976
Congenital enzymopenic methaemoglobinaemia. Clinical and biochemical study of a family with three homozygotes
A Mast, R Milo, C Junien, et al.
Human Genetics
|
January 1, 1983
Four new haplotypes observed in Algerian beta-thalassemia patients
C Beldjord, C Lapouméroulie, M L Baird, et al.
Gene
|
June 19, 1998
Diversity of sequence haplotypes associated with beta-thalassaemia mutations in Algeria: implications for their origin
P Perrin, R Bouhassa, L Mselli, et al.
American Journal of Human Genetics
|
July 1, 1989
Nucleotide variations in the 3' A gamma enhancer region are linked to beta-gene cluster haplotypes and are unrelated to fetal hemoglobin expression
A Ragusa, M Lombardo, E Bouhassira, et al.
Progress in Clinical and Biological Research
|
January 1, 1989
Sequence variations in the 3' A gamma enhancer are silent polymorphisms
A Ragusa, M Lombardo, T Lombardo, et al.
Human Genetics
|
June 1, 1993
Inter-ethnic polymorphism of the beta-globin gene locus control region (LCR) in sickle-cell anemia patients
B Périchon, A Ragusa, C Lapouméroulie, et al.
The Journal of Clinical Endocrinology and Metabolism
|
August 1, 1983
Influence of thyroid status on hemoglobin A2 expression
J M Kuhn, M Rieu, J Rochette, et al.
Human Genetics
|
January 1, 1984
alpha-Thalassemia among sickle cell anemia patients in various African populations
J Pagnier, O Dunda-Belkhodja, I Zohoun, et al.
American Journal of Hematology
|
July 1, 1991
Preliminary report on the use of desferrioxamine in the treatment of Plasmodium falciparum malaria
O Traore, P Carnevale, L Kaptue-Noche, et al.
Page
of 22