Identification of a 220-kb insertion into the Duchenne gene in a family with an atypical course of muscular dystrophy
Author:
Publisher
Elsevier BV
Subject
Genetics
Reference22 articles.
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2. Localisation of Xp21 meiotic exchange points in Duchenne muscular dystrophy families;Bertelson;J. Med. Genet,1986
3. Long-range restriction map around the Duchenne muscular dystrophy gene;Burmeister;Nature (London),1986
4. A 10-megabase physical map of human Xp21, including the Duchenne muscular dystrophy gene;Burmeister;Genomics,1988
5. An insertion within the factor IX gene: Hemophilia BEl Salvadur;Chen;Amer. J. Hum. Genet,1988
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1. Duchenne and Becker Muscular Dystrophies;Neurologic Clinics;2014-08
2. Detection of microdeletions in the short arm of the X chromosome by chromosome stretching;Cytogenetic and Genome Research;2001
3. Elevated p21 mRNA level in skeletal muscle of DMD patients and mdx mice indicates either an exhausted satellite cell pool or a higher p21 expression in dystrophin-deficient cells per se;Journal of Molecular Medicine;2000-11-09
4. Muskeldystrophien;Monogen bedingte Erbkrankheiten 1;2000
5. Aktuelle Diagnostik bei Muskeldystrophien;Der Nervenarzt;1999-02-09
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