Clinical phenotype in congenital muscular dystrophy: correlation with expression of merosin in skeletal

Author:

Philpot J.,Sewry C.,Pennock J.,Dubowitz V.

Publisher

Elsevier BV

Subject

Genetics (clinical),Neurology (clinical),Neurology,Pediatrics, Perinatology and Child Health

Reference12 articles.

1. Muscle Disorders in Childhood;Dubowitz,1994

2. Congenital muscular dystrophy and cerebral CT scan anomalies;Echenne;J Neurol Sci,1986

3. Occidental type cerebromuscular dystrophy: a report of eleven cases;Topaloglu;J Neurol Neurosurg Psychiatr,1991

4. Workshop report on 22nd ENMC sponsored meeting on congenital muscular dystrophy held in Baarn;Dubowitz,1994

5. Familial concordance of brain magnetic resonance imaging changes in congenital muscular dystrophy;Philpot;Neuromusc Disord,1995

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