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American Journal of Human Genetics|March 21, 2000
Assignment of a form of congenital muscular dystrophy with secondary merosin deficiency to chromosome 1q42M Brockington, C A Sewry, R Herrmann, et al.Journal of Medical Genetics|September 1, 1995
The myotubular myopathies: differential diagnosis of the X linked recessive, autosomal dominant, and autosomal recessive forms and present state of DNA studiesC Wallgren-Pettersson, A Clarke, F Samson, et al.Lancet (London, England)|March 2, 1996
Diagnosis of merosin (laminin-2) deficient congenital muscular dystrophy by skin biopsyC A Sewry, J Philpot, L M Sorokin, et al.Neuropediatrics|August 1, 1997
Expression of laminin chains in skin in merosin-deficient congenital muscular dystrophyC A Sewry, M D'Alessandro, L A Wilson, et al.Comptes Rendus De L'Academie Des Sciences. Serie III, Sciences De La Vie|December 1, 1995
Readjusting the localization of merosin (laminin alpha 2-chain) deficient congenital muscular dystrophy locus on chromosome 6q2A Helbling-Leclerc, H Topaloglu, F M Tomé, et al.Neuromuscular Disorders : NMD|March 1, 1993
Manifesting carriers of Xp21 muscular dystrophy; lack of correlation between dystrophin expression and clinical weaknessC A Sewry, A Sansome, A Clerk, et al.Developmental Medicine and Child Neurology|December 1, 1991
A new system for cotside display and analysis of the preterm neonatal electroencephalogramD F Wertheim, D G Murdoch Eaton, R C Oozeer, et al.Neuromuscular Disorders : NMD|June 3, 1998
Early presentation of X-linked Emery-Dreifuss muscular dystrophy resembling limb-girdle muscular dystrophyF Muntoni, E J Lichtarowicz-Krynska, C A Sewry, et al.Human Molecular Genetics|October 1, 1994
Deficiency of the human mitochondrial transcription factor h-mtTFA in infantile mitochondrial myopathy is associated with mtDNA depletionJ Poulton, K Morten, C Freeman-Emmerson, et al.Human Immunology|May 1, 1988
C4 complement allotypes in juvenile dermatomyositisS A Robb, A H Fielder, C E Saunders, et al.Pageof 24