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Proceedings of the National Academy of Sciences of the United States of America|April 1, 1985
Common haplotype dependency of high G gamma-globin gene expression and high Hb F levels in beta-thalassemia and sickle cell anemia patientsD Labie, J Pagnier, C Lapoumeroulie, et al.American Journal of Human Genetics|April 1, 1997
A gene for dominant nonspecific X-linked mental retardation is located in Xq28V des Portes, P Billuart, A Carrié, et al.Revue Neurologique|September 24, 2008
[Epileptogenic brain malformations: radiological and clinical presentation and indications for genetic testing]N Bahi-Buisson, N Boddaert, Y Saillour, et al.American Journal of Medical Genetics|October 23, 1997
Gene for nonspecific X-linked mental retardation (MRX 47) is located in Xq22.3-q24V des Portes, N Soufir, A Carrié, et al.Annales De Genetique|January 1, 1997
Molecular diagnosis of congenital bilateral absence of the vas deferens: analyses of the CFTR gene in 64 French patientsT Bienvenu, M Adjiman, N Thiounn, et al.Clinical Genetics|June 4, 1998
Inherited microdeletion in Xp21.3-22.1 involved in non-specific mental retardationV des Portes, A Carrié, P Billuart, et al.Human Molecular Genetics|May 18, 2000
MECP2 mutations account for most cases of typical forms of Rett syndromeT Bienvenu, A Carrié, N de Roux, et al.Annales De Biologie Clinique|August 10, 2000
[Molecular analysis and prenatal diagnosis of beta-thalassemia: about our experience in central Tunisia]S Laradi, A Haj Khelil, H Omri, et al.Proceedings of the National Academy of Sciences of the United States of America|July 22, 1998
Somatic mutations of the beta-catenin gene are frequent in mouse and human hepatocellular carcinomasA de La Coste, B Romagnolo, P Billuart, et al.Human Molecular Genetics|July 1, 1996
Identification by STS PCR screening of a microdeletion in Xp21.3-22.1 associated with non-specific mental retardationP Billuart, M C Vinet, V des Portes, et al.Pageof 8