Showing results (201-210 of 214) with videos related to
Sort By:
Pageof 22
Human Molecular Genetics|March 21, 1998
Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophyL Cartegni, M R di Barletta, R Barresi, et al.Annals of Neurology|August 1, 1997
X-linked Emery-Dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sampleM Mora, L Cartegni, C Di Blasi, et al.Nature Genetics|March 18, 1999
Mutations in the gene encoding lamin A/C cause autosomal dominant Emery-Dreifuss muscular dystrophyG Bonne, M R Di Barletta, S Varnous, et al.Human Reproduction (Oxford, England)|September 4, 2021
Targeted whole exome sequencing and Drosophila modelling to unveil the molecular basis of primary ovarian insufficiencyI Bestetti, C Barbieri, A Sironi, et al.Nature Genetics|June 10, 1998
Mutations in GDI1 are responsible for X-linked non-specific mental retardationP D'Adamo, A Menegon, C Lo Nigro, et al.American Journal of Human Genetics|October 23, 1997
The X-linked gene G4.5 is responsible for different infantile dilated cardiomyopathiesP D'Adamo, L Fassone, A Gedeon, et al.Human Molecular Genetics|July 21, 1998
Non-specific X-linked semidominant mental retardation by mutations in a Rab GDP-dissociation inhibitorT Bienvenu, V des Portes, A Saint Martin, et al.Human Reproduction (Oxford, England)|October 2, 2004
Mutation analysis of two candidate genes for premature ovarian failure, DACH2 and POF1BS Bione, F Rizzolio, C Sala, et al.American Journal of Human Genetics|March 31, 2000
Different mutations in the LMNA gene cause autosomal dominant and autosomal recessive Emery-Dreifuss muscular dystrophyM Raffaele Di Barletta, E Ricci, G Galluzzi, et al.Annals of Neurology|August 12, 2000
Clinical and molecular genetic spectrum of autosomal dominant Emery-Dreifuss muscular dystrophy due to mutations of the lamin A/C geneG Bonne, E Mercuri, A Muchir, et al.Pageof 22