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Neuromuscular Disorders : NMD|November 23, 2006
Mutation analysis in the FKRP gene provides an explanation for a rare cause of intrafamilial clinical variability in LGMD2IN M Vieira, D Schlesinger, F de Paula, et al.
Growth Regulation|March 1, 1991
Short stature in Duchenne muscular dystrophyD Rapaport, G M Colletto, M Vainzof, et al.
Journal of Medical Genetics|January 1, 1995
Myotonic dystrophy: genetic, clinical, and molecular analysis of patients from 41 Brazilian familiesM R Passos-Bueno, A Cerqueira, M Vainzof, et al.
Journal of Medical Genetics|July 1, 1992
A model to estimate the expression of the dystrophin gene in muscle from female Becker muscular dystrophy carriersM Vainzof, M R Passos-Bueno, R C Pavanello, et al.
American Journal of Medical Genetics|August 1, 1989
Nocturnal rhythm of growth hormone in Duchenne patients: effect of different doses of mazindol and/or cyproheptadineM Zatz, D Rapaport, R C Pavanello, et al.
American Journal of Medical Genetics|June 15, 1991
Apparent association of mental retardation and specific patterns of deletions screened with probes cf56a and cf23a in Duchenne muscular dystrophyD Rapaport, M R Passos-Bueno, L Brandão, et al.
Neurology|December 14, 2005
A family with McLeod syndrome and calpainopathy with clinically overlapping diseasesA Starling, D Schlesinger, F Kok, et al.
Human Molecular Genetics|January 1, 1993
Is the maintainance of the C-terminus domain of dystrophin enough to ensure a milder Becker muscular dystrophy phenotype?M Vainzof, R I Takata, M R Passos-Bueno, et al.
American Journal of Medical Genetics|March 17, 2001
Mutations in the caveolin-3 gene: When are they pathogenic?F de Paula, M Vainzof, A L Bernardino, et al.
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