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Cancer Genetics and Cytogenetics|June 1, 1992
Structural rearrangements of chromosome 13 as additional abnormalities in Burkitt lymphoma and type 3 acute lymphoblastic leukemiaC Barin, C Valtat, S Briault, et al.Archives De Pediatrie : Organe Officiel De La Societe Francaise De Pediatrie|January 17, 2012
[Diagnostic investigations for an unexplained developmental disability]A Verloes, D Héron, T Billette de Villemeur, et al.Revue Francaise De Gynecologie Et D'Obstetrique|October 1, 1984
[Should we still explore placental sulfatase deficiencies? Reflections apropos of a case report]Y Giovangrandi, G Magnin, E Sauvanet, et al.American Journal of Medical Genetics|May 8, 1999
X-linked nonspecific mental retardation (MRX16) mapping to distal Xq28: linkage study and neuropsychological data in a large familyC Gendrot, N Ronce, M Raynaud, et al.Human Genetics|February 1, 1997
Nance-Horan syndrome: linkage analysis in 4 families refines localization in Xp22.31-p22.13 regionA Toutain, N Ronce, B Dessay, et al.Clinical Genetics|March 1, 1994
X-linked mental retardation exhibiting linkage to DXS255 and PGKP1: a new MRX family (MRX14) with localization in the pericentromeric regionC Gendrot, N Ronce, A Toutain, et al.American Journal of Human Genetics|October 1, 1990
Definitive localization of X-linked Kallman syndrome (hypogonadotropic hypogonadism and anosmia) to Xp22.3: close linkage to the hypervariable repeat sequence CRI-S232T Meitinger, B Heye, C Petit, et al.Annales De Genetique|May 20, 2000
Determination of the gene structure of human oligophrenin-1 and identification of three novel polymorphisms by screening of DNA from 164 patients with non-specific X-linked mental retardationP Billuart, J Chelly, A Carrié, et al.Journal of Neuropathology and Experimental Neurology|August 14, 1999
Expression of FMR1, FXR1, and FXR2 genes in human prenatal tissuesC Agulhon, P Blanchet, A Kobetz, et al.Archives Des Maladies Du Coeur Et Des Vaisseaux|February 24, 2005
[Apical left ventricular aneurysm without atrio-ventricular block due to a lamin A/C gene mutation]J E Forissier, G Bonne, C Bouchier, et al.Pageof 11