Showing results (191-200 of 240) with videos related to
Sort By:
Pageof 24
Neuromuscular Disorders : NMD|May 1, 1994
Infantile axonal neuropathy in two siblingsR M Quinlivan, S A Robb, S M Hall, et al.Neuromuscular Disorders : NMD|May 1, 1997
Prenatal diagnosis in merosin-deficient congenital muscular dystrophyI Naom, C Sewry, M D'Alessandro, et al.Neuromuscular Disorders : NMD|December 1, 1996
Sequential study of central and peripheral nervous system involvement in an infant with merosin-deficient congenital muscular dystrophyE Mercuri, J Pennock, F Goodwin, et al.Brain : a Journal of Neurology|December 28, 1999
Mutations in the laminin alpha2-chain gene in two children with early-onset muscular dystrophyI Naom, M D'alessandro, C A Sewry, et al.Neuromuscular Disorders : NMD|January 1, 1992
Linkage of Emery-Dreifuss muscular dystrophy to the red/green cone pigment (RGCP) genes, proximal to factor VIIIC G Cole, S J Abbs, V Dubowitz, et al.Proceedings of the National Academy of Sciences of the United States of America|February 1, 1984
Monoclonal antibodies detect a spectrin-like protein in normal and dystrophic human skeletal muscleS T Appleyard, M J Dunn, V Dubowitz, et al.Journal of Medical Genetics|February 1, 1996
Gene deletions in spinal muscular atrophyN R Rodrigues, N Owen, K Talbot, et al.Neuromuscular Disorders : NMD|March 1, 1997
Late onset muscular dystrophy with cerebral white matter changes due to partial merosin deficiencyE Tan, H Topaloglu, C Sewry, et al.Neuromuscular Disorders : NMD|May 1, 1997
Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chainC A Sewry, I Naom, M D'Alessandro, et al.Journal of Medical Genetics|December 1, 1986
The screening of Duchenne muscular dystrophy patients for submicroscopic deletionsK Hart, C Cole, A Walker, et al.Pageof 24