Molecular analysis of human muscular dystrophies-Reference-Cited by-同舟云学术

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Molecular analysis of human muscular dystrophies

Published:1987-03 Issue:3 Volume:10 Page:191-199
ISSN:0148-639X
Container-title:Muscle & Nerve
language:en
Short-container-title:Muscle Nerve

Author:

Davies K. E.,Forrest S.,Smith T.,Kenwrick S.,Ball S.,Dorkins H.,Patterson M.

Publisher

Wiley

Subject

Physiology (medical),Cellular and Molecular Neuroscience,Clinical Neurology,Physiology

Reference44 articles.

1. Delayed cutaneous hypersensitivity in rheumatoid arthritis: The influence of nutrition and drug therapy

2. PRENATAL DIAGNOSIS AND CARRIER DETECTION OF DUCHENNE MUSCULAR DYSTROPHY WITH CLOSELY LINKED RFLPs

3. A glyceraldehyde-3-phosphate dehydrogenase pseudogene on the short arm of the human X chromosomes defines a multigene family.

4. Mapping genetic markers on human chromosome 19 using subchromosomal fragments in somatic cell hybrids

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. Review Article: Dystrophin-Related Muscular Dystrophies;Journal of Child Neurology;1989-10

2. The pathological damage in duchenne muscular dystrophy may be due to increased intracellular oxy-radical generation caused by the absence of dystrophin and subsequent alterations in Ca2+ metabolism;Medical Hypotheses;1989-07

3. Treatment of muscular dystrophies;General Pharmacology: The Vascular System;1989-01

4. Rehabilitation of Infants and Children with Neuromuscular Disorders;Pediatric Annals;1988-12

5. A double-blind placebo controlled trial of diltiazem in duchenne dystrophy;Klinische Wochenschrift;1988-07

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