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Journal of Medical Genetics|March 1, 1987
The application of linkage analysis to genetic counselling in families with Duchenne or Becker muscular dystrophyS Hodgson, A Walker, C Cole, et al.
Neuromuscular Disorders : NMD|January 1, 1992
Correlation of clinical and deletion data in Duchenne and Becker muscular dystrophy, with special reference to mental abilityS V Hodgson, S Abbs, S Clark, et al.
Neuromuscular Disorders : NMD|June 6, 2000
High resolution magnetic resonance imaging of the brain in the dy/dy mouse with merosin-deficient congenital muscular dystrophyD J Dubowitz, J M Tyszka, C A Sewry, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|October 26, 1981
Activity of creatine kinase in sera from healthy women, carriers of Duchenne muscular dystrophy and cord blood, determined by the "European" recommended method with NAC-EDTA activationD W Moss, K B Whitaker, C Parmar, et al.
AJNR. American Journal of Neuroradiology|January 1, 1987
Serial MR imaging in neonatal cerebral injuryM A Johnson, J M Pennock, G M Bydder, et al.
Biochemical Society Symposium|January 1, 1987
The role of Coxsackie B viruses in the pathogenesis of myocarditis, dilated cardiomyopathy and inflammatory muscle diseaseL C Archard, P J Richardson, E G Olsen, et al.
American Journal of Medical Genetics|August 28, 1995
Characterization of genetic deletions in Becker muscular dystrophy using monoclonal antibodies against a deletion-prone region of dystrophinLe Thiet Thanh, Nguyen Thi Man, S Hori, et al.
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.
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