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Clinical Genetics|October 27, 1998
Severe classical congenital muscular dystrophy and merosin expressionJ Vajsar, D Chitayat, L E Becker, et al.Pediatric Neurology|March 30, 2000
Basal lamina abnormality in the skeletal muscle of Walker-Warburg syndromeJ Vajsar, C Ackerley, D Chitayat, et al.Journal of Child Neurology|March 12, 1999
Cardiac manifestations of congenital fiber-type disproportion myopathyB L Banwell, L E Becker, V Jay, et al.Pediatric Neurology|April 1, 1995
Arthrogryposis multiplex congenita due to congenital myasthenic syndromeJ Vajsar, A Sloane, D L MacGregor, et al.Brain & Development|September 1, 1996
Infantile myositis presenting in the neonatal periodJ Vajsar, V Jay, P BabynBrain & Development|January 1, 1997
Giant cells in cortical tubers in tuberous sclerosis showing synaptophysin-immunoreactive halosH Yamanouchi, M Ho, V Jay, et al.American Journal of Medical Genetics|January 2, 1996
Terminal deletion of the long arm of chromosome 3 [46,XX,del(3)(q27-->qter)]D Chitayat, R Babul, M M Silver, et al.Pediatric and Developmental Pathology : the Official Journal of the Society for Pediatric Pathology and the Paediatric Pathology Society|December 16, 1998
Gonadoblastoid testicular dysplasia in Walker-Warburg syndromeN A Hung, M M Silver, D Chitayat, et al.Archives of Pathology & Laboratory Medicine|September 1, 1994
Fiber-type differentiation by myosin immunohistochemistry on paraffin-embedded skeletal muscle. A useful adjunct to fiber typing by the adenosine triphosphatase reactionV Jay, L E BeckerPageof 286