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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 Lapouméroulie
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.
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 Genetics|March 1, 1997
Molecular basis of alpha-thalassemia in SicilyM Fichera, A Spalletta, F Fiorenza, et al.
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