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Showing results (171-180 of 212) with videos related to

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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 traitC Junien, A Chaventré, Y Fofana, et al.
Acta Haematologica|January 1, 1976
Congenital enzymopenic methaemoglobinaemia. Clinical and biochemical study of a family with three homozygotesA Mast, R Milo, C Junien, et al.
Human Genetics|January 1, 1983
Four new haplotypes observed in Algerian beta-thalassemia patientsC 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 originP 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 expressionA 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 polymorphismsA 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 patientsB Périchon, A Ragusa, C Lapouméroulie, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1983
Influence of thyroid status on hemoglobin A2 expressionJ M Kuhn, M Rieu, J Rochette, et al.
Human Genetics|January 1, 1984
alpha-Thalassemia among sickle cell anemia patients in various African populationsJ 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 malariaO Traore, P Carnevale, L Kaptue-Noche, et al.
Pageof 22

Showing results (171-180 of 212) with videos related to

Sort By:
Pageof 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 traitC Junien, A Chaventré, Y Fofana, et al.
Acta Haematologica|January 1, 1976
Congenital enzymopenic methaemoglobinaemia. Clinical and biochemical study of a family with three homozygotesA Mast, R Milo, C Junien, et al.
Human Genetics|January 1, 1983
Four new haplotypes observed in Algerian beta-thalassemia patientsC 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 originP 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 expressionA 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 polymorphismsA 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 patientsB Périchon, A Ragusa, C Lapouméroulie, et al.
The Journal of Clinical Endocrinology and Metabolism|August 1, 1983
Influence of thyroid status on hemoglobin A2 expressionJ M Kuhn, M Rieu, J Rochette, et al.
Human Genetics|January 1, 1984
alpha-Thalassemia among sickle cell anemia patients in various African populationsJ 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 malariaO Traore, P Carnevale, L Kaptue-Noche, et al.
Pageof 22