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European Journal of Human Genetics : EJHG|July 21, 2001
No mutations in the coding region of the Rett syndrome gene MECP2 in 59 autistic patientsP Vourc'h, T Bienvenu, C Beldjord, et al.Nature|June 20, 1991
Uniparental paternal disomy in a genetic cancer-predisposing syndromeI Henry, C Bonaiti-Pellié, V Chehensse, et al.Blood|December 1, 1985
The -158 site 5' to the G gamma gene and G gamma expressionD Labie, O Dunda-Belkhodja, F Rouabhi, et al.Nouvelle Revue Francaise D'Hematologie|January 1, 1984
[Erythrocytosis due to a high-affinity hemoglobulin: mutant hemoglobin Saint-Jacques beta 140 (H18) Ala----Thr with a change in the 2,3-diphosphoglycerate binding site]J Rochette, J P Boissel, D Labie, et al.The Journal of Clinical Investigation|July 1, 1981
Impairment of the growth of Plasmodium falciparum in HbEE erythrocytesR L Nagel, C Raventos-Suarez, M E Fabry, et al.Anemia|July 26, 2012
Foetal haemoglobin, erythrocytes containing foetal haemoglobin, and hematological features in congolese patients with sickle cell anaemiaL Tshilolo, V Summa, C Gregorj, et al.The New England Journal of Medicine|April 4, 1985
Hematologically and genetically distinct forms of sickle cell anemia in Africa. The Senegal type and the Benin typeR L Nagel, M E Fabry, J Pagnier, et al.Human Genetics|August 4, 2005
Maternal mosaicism for mutations in the ARX gene in a family with X linked mental retardationK Poirier, J Abriol, I Souville, et al.American Journal of Hematology|July 1, 1992
Genetic epidemiology of beta-thalassemia in Sicily: do sequences 5' to the G gamma gene and 5' to the beta gene interact to enhance HbF expression in beta-thalassemia?A Ragusa, M Lombardo, C Beldjord, et al.The Journal of Clinical Investigation|September 1, 1981
Sickle gene. Its origin and diffusion from West AfricaJ G Mears, H M Lachman, R Cabannes, et al.Pageof 20