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D Labie

Showing results (121-130 of 212) with videos related to

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Hemoglobin|January 1, 1976
A second case of hemoglobin Grady, repetitive in the middle of the alpha chainD Labie, O Bertrand, O Belkhodja, et al.
Acta Haematologica|January 1, 1987
Haemoglobin disorders among Southeast-Asian refugees in FranceC Dode, A Berth, F Bourdillon, et al.
Human Genetics|August 1, 1992
A haplotype-linked four base pair deletion upstream of the A gamma globin gene coincides with decreased gene expressionC Beldjord, R Ducrocq, S Nadifi, et al.
Lancet (London, England)|August 27, 1983
Haplotype-VI-associated mild beta +-thalassemia in Sicily: Mediterranean type?C Troungos, G Sartino, R Cacciola, et al.
Nouvelle Revue Francaise D'Hematologie|July 1, 1972
[Clinical tribulations of Toulouse I hemoglobin]R Biermé, D Labie, J Rosa, et al.
Archives Francaises De Pediatrie|August 1, 1987
[Influence of alpha-thalassemia on the hematologic expression of homozygote drepanocytosis]M de Montalembert, C Dode, M Maier-Redelsperger, et al.
Presse Medicale (Paris, France : 1983)|May 20, 1989
[Treatment of homozygote beta thalassemia in Algiers. A 5-year follow-up of 66 patients]L Adjrad, A Amara, F Rouabhi, et al.
The Journal of Clinical Investigation|June 1, 1989
A gene conversion located 5' to the A gamma gene in linkage disequilibrium with the Bantu haplotype in sickle cell anemiaE E Bouhassira, H Lachman, R Krishnamoorthy, et al.
Diabete & Metabolisme|June 1, 1981
Minor haemoglobin fractions in uraemic and in diabetic patientsB Lantz, H Wajcman, M Beaufils, et al.
Biochimica Et Biophysica Acta|January 25, 1977
Hemoglobin Djelfa beta98 (FG 5) Val leads to Ala: isolation and functional properties of the heme saturated formG Gacon, R Krishnamoorthy, H Wajcman, et al.
Pageof 22

Showing results (121-130 of 212) with videos related to

Sort By:
Pageof 22
Hemoglobin|January 1, 1976
A second case of hemoglobin Grady, repetitive in the middle of the alpha chainD Labie, O Bertrand, O Belkhodja, et al.
Acta Haematologica|January 1, 1987
Haemoglobin disorders among Southeast-Asian refugees in FranceC Dode, A Berth, F Bourdillon, et al.
Human Genetics|August 1, 1992
A haplotype-linked four base pair deletion upstream of the A gamma globin gene coincides with decreased gene expressionC Beldjord, R Ducrocq, S Nadifi, et al.
Lancet (London, England)|August 27, 1983
Haplotype-VI-associated mild beta +-thalassemia in Sicily: Mediterranean type?C Troungos, G Sartino, R Cacciola, et al.
Nouvelle Revue Francaise D'Hematologie|July 1, 1972
[Clinical tribulations of Toulouse I hemoglobin]R Biermé, D Labie, J Rosa, et al.
Archives Francaises De Pediatrie|August 1, 1987
[Influence of alpha-thalassemia on the hematologic expression of homozygote drepanocytosis]M de Montalembert, C Dode, M Maier-Redelsperger, et al.
Presse Medicale (Paris, France : 1983)|May 20, 1989
[Treatment of homozygote beta thalassemia in Algiers. A 5-year follow-up of 66 patients]L Adjrad, A Amara, F Rouabhi, et al.
The Journal of Clinical Investigation|June 1, 1989
A gene conversion located 5' to the A gamma gene in linkage disequilibrium with the Bantu haplotype in sickle cell anemiaE E Bouhassira, H Lachman, R Krishnamoorthy, et al.
Diabete & Metabolisme|June 1, 1981
Minor haemoglobin fractions in uraemic and in diabetic patientsB Lantz, H Wajcman, M Beaufils, et al.
Biochimica Et Biophysica Acta|January 25, 1977
Hemoglobin Djelfa beta98 (FG 5) Val leads to Ala: isolation and functional properties of the heme saturated formG Gacon, R Krishnamoorthy, H Wajcman, et al.
Pageof 22