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Human Genetics|January 1, 1984
Hemoglobins S and C in Upper VoltaD Labie, C Richin, J Pagnier, et al.
Haematologia|January 1, 1988
Density distribution of red cells and prognostic significance in 50 patients with homozygous sickle-cell diseaseN Pajot, M Maier-Redelsperger, C Dode, et al.
Presse Medicale (Paris, France : 1983)|November 30, 1985
[Homozygous beta-thalassemia in Algeria. Study of 50 cases]L Adjrad, F Rouabhi, A Amara, et al.
Biochemistry|November 4, 1975
Isolation and functional characterization of hemoglobin Casper: beta106(G8) Leu replaced by ProH Wajcman, G Gacon, D Labie, et al.
Human Genetics|January 1, 1984
A leftward deletional alpha+ thalassemia found in East Sicily in conjunction with heterozygous beta-thalassemiaC Troungos, R Krishnamoorthy, T Lombardo, et al.
Nucleic Acids Research|October 26, 1987
Expression of a beta thalassemia gene with abnormal splicingC Lapoumeroulie, S Acuto, F Rouabhi, et al.
Acta Haematologica|January 1, 1987
Haemoglobin disorders among Southeast-Asian refugees in FranceC Dode, A Berth, F Bourdillon, 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.
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