INHERITED DELETION AT DUCHENNE DYSTROPHY LOCUS IN NORMAL MALE
Author:
Publisher
Elsevier BV
Subject
General Medicine
Reference6 articles.
1. Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organisation of the DMD gene in normal and affected individuals;Koenig;Cell,1987
2. A cDNA clone from the Duchenne/Becker muscular dystrophy gene;Burghes;Nature,1987
3. Duchenne muscular dystrophy: high frequency of deletions;Bartlett;Neurology,1988
4. Inherited deletion at Duchenne dystrophy locus in normal male;Koh;Lancet,1987
5. Ng Laing, et al., Duchenne muscular dystrophy: detection of deletion carriers by spectrophotometric densitometry, Clin Genet ((in press)).
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1. Similarity of DMD gene deletion and duplication in the Chinese patients compared to global populations;Behavioral and Brain Functions;2008-04-29
2. MLPA analysis for the detection of deletions, duplications and complex rearrangements in the dystrophin gene: potential and pitfalls;Neurogenetics;2005-01-18
3. The milder phenotype of the dystrophin gene double deletions;Acta Neurologica Scandinavica;2003-05-20
4. A Double-Deletion Mutation in the Pitx3 Gene Causes Arrested Lens Development in Aphakia Mice;Genomics;2001-02
5. Muscular dystrophy: Centronucleation may reflect a compensatory activation of defective myonuclei;Journal of Biomedical Science;1998-01
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