Molecular analysis of Duchenne and Becker muscular dystrophy
Author:
Publisher
Wiley
Subject
General Biochemistry, Genetics and Molecular Biology
Reference30 articles.
1. & (1983). The muscular dystrophies. In The Metabolic Basis of Inherited Disease (ed. J. B. Stanburg, J. B. Wyngaarden, D. S. Frederickson, J. L. Goldstein & M. S. Brown), 5th ed., pp. 1470-1495.
2. Duchenne muscular dystrophy: Pathogenetic aspects and genetic prevention
3. Expression of an X-linked muscular dystrophy in a female due to translocation involving Xp21 and non-random inactivation of the normal X chromosome
4. Muscular dystrophy in an X; 1 translocation female suggests that Duchenne locus is on X chromosome short arm.
Cited by 5 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. Report of the DNA committee and catalogues of cloned and mapped genes and DNA polymorphisms;Cytogenetic and Genome Research;1990
2. Calcium regulation in muscle diseases; the influence of innervation and activity;Biochimica et Biophysica Acta (BBA) - General Subjects;1989-05
3. Carrier detection and prenatal diagnosis in Duchenne and Becker mucualr dystrophy;British Medical Bulletin;1989
4. GENETICS OF DUCHENNE MUSCULAR DYSTROPHY;Annual Review of Genetics;1988-12
5. GENE STUDIES IN NEWBORN MALES WITH DUCHENNE MUSCULAR DYSTROPHY DETECTED BY NEONATAL SCREENING;The Lancet;1988-08
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