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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.Human Biology|December 1, 1992
Importation route of the sickle cell trait into Portugal: contribution of molecular epidemiologyJ Lavinha, J Gonçalves, P Faustino, 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.Nature|February 28, 1980
Beta-chain contact sites in the haemoglobin S polymerR L Nagel, J Johnson, R M Bookchin, 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.American Journal of Hematology|December 12, 1997
Dissection of the association status of two polymorphisms in the beta-globin gene cluster with variations in F-cell number in non-anemic individualsT Merghoub, B Perichon, M Maier-Redelsperger, 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.Pageof 20