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Journal article

Localization and cloning of Xp21 deletion breakpoints involved in muscular dystrophy.

Abstract:

Twenty-nine deletion breakpoints were mapped in 220 kb of the DXS164 locus relative to potential exons of the Duchenne and Becker muscular dystrophy gene. Four deletion junction fragments were isolated to acquire outlying Xp21 loci on both the terminal and centromere side of the DXS164 locus. The junction loci were used for chromosome walking, searches for DNA polymorphisms, and mapping against deletion and translocation breakpoints. Forty-four unrelated deletions were analyzed using the junc...

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Publication status:
Published

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Publisher copy:
10.1007/bf00281063

Authors


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Institution:
University of Oxford
Department:
Oxford, MSD, Clinical Medicine, WTC Human Genetics
Bertelson, CJ More by this author
Colletti-Feener, C More by this author
Kunkel, LM More by this author
Publisher:
Springer-Verlag
Journal:
Human genetics
Volume:
75
Issue:
3
Pages:
221-227
Publication date:
1987-03-05
DOI:
EISSN:
1432-1203
ISSN:
0340-6717
URN:
uuid:ae422a5e-2ed2-452c-8465-f6d0d4901281
Source identifiers:
115663
Local pid:
pubs:115663

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