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Circulation|October 15, 1996
Failure to detect connexin43 mutations in 38 cases of sporadic and familial heterotaxyM Gebbia, J A Towbin, B CaseyToxicology|July 17, 1989
Interactions of manganese with human brain glutathione-S-transferaseA Vescovi, M Gebbia, G Cappelletti, et al.Neuromuscular Disorders : NMD|July 1, 1995
Lack of mRNA and dystrophin expression in DMD patients three months after myoblast transferL Morandi, P Bernasconi, M Gebbia, et al.Journal of Neuroimmunology|August 1, 1996
Major histocompatibility complex class II molecule expression on muscle cells is regulated by differentiation: implications for the immunopathogenesis of muscle autoimmune diseasesR Mantegazza, M Gebbia, M Mora, et al.Neuromuscular Disorders : NMD|January 1, 1993
Very small dystrophin molecule in a family with a mild form of Becker dystrophyL Morandi, M Mora, P Bernasconi, et al.American Journal of Medical Genetics|January 23, 1999
Left-right axis malformations associated with mutations in ACVR2B, the gene for human activin receptor type IIBR Kosaki, M Gebbia, K Kosaki, et al.Journal of Neurology|September 1, 1993
Dystrophin abnormalities in Duchenne and Becker dystrophy carriers: correlation with cytoskeletal proteins and myosinsM Mora, L Morandi, A Piccinelli, et al.Muscle & Nerve|October 1, 1994
Fetus-like dystrophin expression and other cytoskeletal protein abnormalities in centronuclear myopathiesM Mora, L Morandi, L Merlini, et al.Nature Genetics|May 1, 1995
Cloning of the gene for ocular albinism type 1 from the distal short arm of the X chromosomeM T Bassi, M V Schiaffino, A Renieri, et al.American Journal of Human Genetics|August 1, 1997
A submicroscopic deletion in Xq26 associated with familial situs ambiguusG B Ferrero, M Gebbia, G Pilia, et al.Pageof 2