Chronic proximal spinal muscular atrophy of childhood and adolescence: problems of classification and genetic counselling.

Author:

Hausmanowa-Petrusewicz I,Zaremba J,Borkowska J

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference15 articles.

1. Chronic proximal spinal muscular atrophy of childhood and adolescence: sex influence;Hausmanowa-Petrusewicz, I.; Zaremba, J.; Borkowska, J.; Szirkowiec, W.;J Med Genet,1984

2. Infantile and juvenile spinal muscular atrophy;Hausmanowa-Petrusewicz, I.; Askanas, W.; Badurska, B.;J Neurol Sci,1968

3. Spinal muscular atrophy. Infantile and juvenile type;Hausmanowa-Petrusewicz, I.;Scientific, Technical and Economic Information

4. Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (WerdnigHoffmann disease) and type III (Kugelberg-Welander disease);Fried, K.; Emery, A.E.H.;Clin Genet,1971

5. Mendelian inheritance in man. Catalogs of autosomal dominant, autosomal recessive and X-linked phenotypes;McKusick, V.A.,1983

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