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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.Human Genetics|July 1, 1994
Unexpected inactivation of acceptor consensus splice sequence by a -3 C to T transition in intron 2 of the CFTR geneT Bienvenu, D Hubert, N Fonknechten, et al.Human Heredity|May 1, 1996
A splicing mutation in intron 16 of the cystic fibrosis transmembrane conductance regulator gene, associated with severe disease, is common on Reunion IslandT Bienvenu, F Cartault, F Lesure, et al.Nucleic Acids Research|March 25, 1988
Recovery of functional DNA inserts by electroendosmotic elution during gel electrophoresisH V Tan, A Kitzis, T Berthollet, et al.Human Genetics|February 1, 1986
Heterogeneity of haplotypes among patients with severe Cooley disease in Eastern SicilyM Lombardo, A Ragusa, G Sortino, et al.Human Mutation|January 1, 1993
Simultaneous detection of the two prevalent mutations in the cystic fibrosis gene in Reunion IslandT Bienvenu, S Bousquet, C Herbulot, et al.Journal De Radiologie|October 1, 1984
[Pyknodysostosis. Classical and unusual aspects. Apropos of 7 cases]C Bennani-Smirès, N R el Alamy, N BoucharebPageof 20