Microdeletions in patients with X-linked muscular dystrophy: molecular-clinical correlations
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-0004.1988.tb03424.x/fullpdf
Reference33 articles.
1. Long-range restriction map around the Duchenne muscular dystrophy gene;Burmeister;Nature,1986
2. Regional mapping of coagulation factor IX gene and several unique DNA sequences of the human X chromosome;Camerino;Cytogenet. Cell. Genet.,1984
3. Duchenne muscular dystrophy with adrenal insufficiency and glycerol kinase deficiency: high resolution cytogenetic analysis with molecular, biochemical, and clinical studies;Clarke;J. Med. Genet.,1986
4. Direct detection of more than 50% of Duchenne muscular dystrophy mutations by field inversion gels;Dunnen;Nature,1987
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1. Genetic and clinical profile of patients of Duchenne muscular dystrophy: Experience from a tertiary care center in Eastern India;Indian Pediatrics;2015-06
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5. Are there ethnic differences in deletions in the dystrophin gene?;American Journal of Medical Genetics;1997-01-20
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