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Medecine Tropicale : Revue Du Corps De Sante Colonial|April 28, 2011
[Pathophysiology of sickle cell disease]J Elion, S Laurance, C LapouméroulieHuman Biology|April 1, 1994
Sequence correction and reassignment of the TaqI polymorphic site in the human inter-gamma-globin gene region, an African-specific markerC Guidal, C Lapouméroulie, R Krishnamoorthy, et al.British Journal of Haematology|September 1, 1982
Homozygous deletional alpha + thalassaemia associated with unequal expression of the two remaining alpha 1 genes (alpha 1A and alpha 1Q)J Pagnier, J Elion, C Lapouméroulie, et al.Human Genetics|September 1, 1992
Analysis of the 5' flanking sequence of the G gamma globin gene by denaturing gradient gel electrophoresis confirms the heterogeneity of the Bantu beta S haplotypeG Tachdjian, M Benabdennebi, C Guidal, et al.Biochemical and Biophysical Research Communications|October 1, 1998
CFTR regions containing duodenum specific DNase I hypersensitive sites drive expression in intestinal crypt cells but not in fibroblastsI Dixméras, C Lapouméroulie, L P Tallec, et al.Human Genetics|January 1, 1983
Four new haplotypes observed in Algerian beta-thalassemia patientsC Beldjord, C Lapouméroulie, M L Baird, et al.Lancet (London, England)|January 26, 2002
A novel mechanism for thalassaemia intermediaC Badens, M G Mattei, A M Imbert, et al.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.Human Genetics|March 1, 1997
Molecular basis of alpha-thalassemia in SicilyM Fichera, A Spalletta, F Fiorenza, et al.Blood|February 1, 1992
DNA sequence variation in a negative control region 5' to the beta-globin gene correlates with the phenotypic expression of the beta s mutationJ Elion, P E Berg, C Lapouméroulie, et al.Pageof 2