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C R Greenberg

Showing results (101-110 of 105) with videos related to

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Neuromuscular Disorders : NMD|October 29, 2000
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)L V Anderson, R M Harrison, R Pogue, et al.
American Journal of Medical Genetics|August 15, 2001
Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophyC A Brown, R W Lanning, K Q McKinney, et al.
Journal of Inherited Metabolic Disease|January 5, 2007
Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)S Kölker, E Christensen, J V Leonard, et al.
American Journal of Human Genetics|October 1, 1989
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletionM Koenig, A H Beggs, M Moyer, et al.
Nature|July 3, 1986
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophyL M Kunkel, J F Hejtmancik, C T Caskey, et al.
Pageof 11

Showing results (101-110 of 105) with videos related to

Sort By:
Pageof 11
You have reached the last page of results.This site can display upto 105 results.
Neuromuscular Disorders : NMD|October 29, 2000
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)L V Anderson, R M Harrison, R Pogue, et al.
American Journal of Medical Genetics|August 15, 2001
Novel and recurrent mutations in lamin A/C in patients with Emery-Dreifuss muscular dystrophyC A Brown, R W Lanning, K Q McKinney, et al.
Journal of Inherited Metabolic Disease|January 5, 2007
Guideline for the diagnosis and management of glutaryl-CoA dehydrogenase deficiency (glutaric aciduria type I)S Kölker, E Christensen, J V Leonard, et al.
American Journal of Human Genetics|October 1, 1989
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletionM Koenig, A H Beggs, M Moyer, et al.
Nature|July 3, 1986
Analysis of deletions in DNA from patients with Becker and Duchenne muscular dystrophyL M Kunkel, J F Hejtmancik, C T Caskey, et al.
Pageof 11