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C Moraine

Showing results (61-70 of 94) with videos related to

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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.
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.
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.
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.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1992
X chromosome-linked Kallmann syndrome: stop mutations validate the candidate geneJ P Hardelin, J Levilliers, I del Castillo, et al.
Pathologie-Biologie|January 14, 1999
Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardationP Billuart, T Bienvenu, N Ronce, et al.
Journal of Medical Genetics|May 15, 2003
Rare polymorphic variants of the AGTR2 gene in boys with non-specific mental retardationT Bienvenu, K Poirier, H Van Esch, et al.
American Journal of Medical Genetics|July 12, 1996
X-linked mental retardation with neonatal hypotonia in a French family (MRX15): gene assignment to Xp11.22-Xp21.1M Raynaud, C Gendrot, B Dessay, et al.
Pageof 10

Showing results (61-70 of 94) with videos related to

Sort By:
Pageof 10
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.
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.
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.
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.
Proceedings of the National Academy of Sciences of the United States of America|September 1, 1992
X chromosome-linked Kallmann syndrome: stop mutations validate the candidate geneJ P Hardelin, J Levilliers, I del Castillo, et al.
Pathologie-Biologie|January 14, 1999
Oligophrenin 1 encodes a rho-GAP protein involved in X-linked mental retardationP Billuart, T Bienvenu, N Ronce, et al.
Journal of Medical Genetics|May 15, 2003
Rare polymorphic variants of the AGTR2 gene in boys with non-specific mental retardationT Bienvenu, K Poirier, H Van Esch, et al.
American Journal of Medical Genetics|July 12, 1996
X-linked mental retardation with neonatal hypotonia in a French family (MRX15): gene assignment to Xp11.22-Xp21.1M Raynaud, C Gendrot, B Dessay, et al.
Pageof 10