Xp21 DNA PROBE IN DIAGNOSIS OF MUSCULAR DYSTROPHY AND SPINAL MUSCULAR ATROPHY
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference4 articles.
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2. Preferential deletion of exons in Duchenne and Becker muscular dystrophies;Forrest;Nature,1987
3. A grandpatemally derived de novo deletion within Xp21 initially presenting in carrier females diagnosed as Kugelberg-Welander syndrome;Wood;Am J Med Genet,1988
4. Becker's X-linked muscular dystrophy: histological, enzyme-histochemical and ultrastructural studies of two cases, originally reported by Becker;Goebel;Acta Neuropathol (Berl),1979
Cited by 6 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. Genetic epidemiology of Duchenne and Becker muscular dystrophy in Slovenia;Clinical Genetics;2008-06-28
2. Inherited Neuronal Atrophy and Degeneration Predominantly of Lower Motor Neurons * *This chapter is reprinted from the third edition because the invited author was unable to meet extended deadlines for revision. A recent review of spinal muscular atrophies by Sabine Rudnik-Schöneborn and colleagues can be found in Myology, third edition, edited by A. G. Engel and C. Franzini-Armstrong (McGraw-Hill, 2004). Several tables from that chapter appear here.;Peripheral Neuropathy;2005
3. Letters to the editor;Muscle & Nerve;1996-04
4. Current Status of Duchenne Muscular Dystrophy;Pediatric Clinics of North America;1992-08
5. Genetic and clinical correlations of Xp21 muscular dystrophy;Journal of Inherited Metabolic Disease;1992-07
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