CARRIER DETECTION AND GENETIC COUNSELLING IN DUCHENNE DYSTROPHY
Author:
Publisher
Wiley
Subject
Clinical Neurology,Developmental Neuroscience,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1975.tb04674.x/fullpdf
Reference36 articles.
1. Myopathic changes in a muscular dystrophy carrier;Dubowitz;Journal of Neurology, Neurosurgery and Psychiatry,1963
2. Clinical manifestations in two carriers of Duchenne muscular dystrophy;Emery;Lancet,1963
3. The manifesting carrier in Ducínenne muscular dystrophy;Moser;Clinical Genetics,1974
4. Mutation rates in Duchenne type of muscular dystrophy;Gardner-Medwin;Journal of Medical Genetics,1970
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3. Muscular Dystrophy;Atlas of Skeletal Muscle Pathology;1985
4. Decrease in the Rate of Protein Synthesis by Polysomes from Cultured Fibroblasts of Patients and Carriers with Duchenne Muscular Dystrophy;Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques;1979-08
5. DETECTION of CARRIERS and GENETIC COUNSELING IN DUCHENNE MUSCULAR DYSTROPHY BY RIBOSOMAL PROTEIN SYNTHESIS;Acta Neurologica Scandinavica;1976-11
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