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Nouvelle Revue Francaise D'Hematologie|January 1, 1981
[Polymorphism of hemoglobins D in Ivory Coast: Hb Korle Bu (beta 73 (E17) Asp leads to Asn), Hb Avicenna (beta 47 (CD6) Asp leads to Ala) and Hb Cocody (beta 21 (B3) Asp leads to Asn) (author's transl)]J P Boissel, H Fabritius, P Richard, et al.
Human Genetics|June 16, 1999
Genetic variations in human fetal globin gene microsatellites and their functional relevanceC Lapoumeroulie, L Castiglia, C Ruberto, et al.
La Semaine Des Hopitaux : Organe Fonde Par L'Association D'Enseignement Medical Des Hopitaux De Paris|April 23, 1977
[Clinical and biological aspects of beta-thalassemia. Apropos of 176 cases]M Belhani, M Dahmane, F Richard, et al.
Blood|August 1, 1977
An unusual case of leukemia with high fetal hemoglobin: demonstration of abnormal hemoglobin synthesis localized in a red cell cloneJ Pagnier, M Lopez, C Mathiot, et al.
Human Genetics|June 1, 1995
Three novel sequence variations in the 5' upstream region of the cystic fibrosis transmembrane conductance regulator (CFTR) gene: two polymorphisms and one putative molecular defectT Bienvenu, V Lacronique, M Raymondjean, et al.
FEBS Letters|December 19, 1994
Cloning and characterization of the human V3 pituitary vasopressin receptorY de Keyzer, C Auzan, F Lenne, et al.
European Journal of Human Genetics : EJHG|January 1, 1996
Analysis of alternative splicing patterns in the cystic fibrosis transmembrane conductance regulator gene using mRNA derived from lymphoblastoid cells of cystic fibrosis patientsT Bienvenu, C Beldjord, J Chelly, et al.
Nouvelle Revue Francaise D'Hematologie|November 25, 1978
[Hemoglobin Pyrgos beta 83 (EF 7) Gly leads to Asp in a Malian: structural identification and functional properties (author's transl)]H Wajcman, G Gacon, C Tudury, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 1, 1988
Structural analysis of the 5' flanking region of the beta-globin gene in African sickle cell anemia patients: further evidence for three origins of the sickle cell mutation in AfricaY Chebloune, J Pagnier, G Trabuchet, et al.
Human Mutation|January 29, 2000
A novel missense mutation D513G in exon 10 of the cystic fibrosis transmembrane conductance regulator (CFTR) gene identified in a French CBAVD patient. Mutations in brief no. 175. OnlineT Bienvenu, S Bousquet, D Vidaud, et al.
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