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Journal of Molecular Neuroscience : MN|October 23, 2001
Dysferlin protein analysis in limb-girdle muscular dystrophiesM Vainzof, L V Anderson, E M McNally, et al.American Journal of Medical Genetics|April 15, 1993
Severe nonspecific X-linked mental retardation caused by a proximally Xp located gene: intragenic heterogeneity or a new form of X-linked mental retardation?M R Passos-Bueno, B C Byth, S Rosenberg, et al.Journal of Child Neurology|April 11, 2000
Heterogeneity of classic congenital muscular dystrophy with involvement of the central nervous system: report of five atypical casesU C Reed, S K Marie, M Vainzof, et al.American Journal of Medical Genetics|March 26, 1998
Social adjustment in adult males affected with progressive muscular dystrophyS Eggers, M ZatzJournal of Neurochemistry|September 1, 1987
Interactions among lithium, calcium, diacylglycerides, and phorbol esters in the regulation of adrenocorticotropin hormone release from AtT-20 cellsT Reisine, M ZatzJournal of Medical Genetics|April 16, 1998
How the magnitude of clinical severity and recurrence risk affects reproductive decisions in adult males with different forms of progressive muscular dystrophyS Eggers, M ZatzNature Genetics|February 2, 2000
Limb-girdle muscular dystrophy type 2G is caused by mutations in the gene encoding the sarcomeric protein telethoninE S Moreira, T J Wiltshire, G Faulkner, et al.Human Heredity|January 1, 1979
A new method for the analysis of age trends in CPK levels with application to Duchenne muscular dystrophyK Lange, M ZatzPageof 26