Diagnosis, Carrier Detection, and Genetic Counseling in the Muscular Dystrophies-Reference-Cited by-同舟云学术

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Diagnosis, Carrier Detection, and Genetic Counseling in the Muscular Dystrophies

Published:1978-08 Issue:3 Volume:25 Page:557-573
ISSN:0031-3955
Container-title:Pediatric Clinics of North America
language:en
Short-container-title:Pediatric Clinics of North America

Author:

Zatz Mayana

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference75 articles.

1. Serum pyruvate kinase in muscle disease and carrier state;Alberts;Neurology,1974

2. Familial muscular dystrophy of late onset;Bacon;J. Neurol. Neurosurg. Psychiatry,1971

3. Eine neue X chromosalmale Muskeldystrophie;Becker;Z. Neurol.,1955

4. Duchenne carrier detection;Danieli;Lancet,1976

5. Early diagnosis and treatment of rapidly developing Duchenne de Boulogne type myopathy;Démos;Am. J. Phys. Med.,1971

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Creatine kinase BB in cerebrospinal fluid and blood: methodology and possible clinical application;Scandinavian Journal of Clinical and Laboratory Investigation;1985-01

2. Myoglobinemia in duchenne muscular;Brain and Development;1980-01

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