Literature DB >> 3587358

Muscular dystrophy: mapping the disease phenotype.

M Robertson.   

Abstract

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Year:  1987        PMID： 3587358     DOI： 10.1038/327372a0

Source DB:  PubMed          Journal:  Nature        ISSN： 0028-0836            Impact factor:   49.962


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  4 in total

1.  Intragenic deletions in 21 Duchenne muscular dystrophy (DMD)/Becker muscular dystrophy (BMD) families studied with the dystrophin cDNA: location of breakpoints on HindIII and BglII exon-containing fragment maps, meiotic and mitotic origin of the mutations.

Authors:  B T Darras; P Blattner; J F Harper; A J Spiro; S Alter; U Francke
Journal:  Am J Hum Genet       Date:  1988-11       Impact factor: 11.025

2.  DNA deletions and recombinations in the gene locus of X-linked muscular dystrophies.

Authors:  M Shimmoto; A Tsuji; R C Yang; Y Nomura; M Segawa; Y Suzuki
Journal:  J Inherit Metab Dis       Date:  1988       Impact factor: 4.982

3.  The use of field-inversion gel electrophoresis for deletion detection in Duchenne muscular dystrophy.

Authors:  J D Chen; M J Denton; G Morgan; J H Pearn; A G Mackinlay
Journal:  Am J Hum Genet       Date:  1988-05       Impact factor: 11.025

4.  Immunological identification of a high molecular weight protein as a candidate for the product of the Duchenne muscular dystrophy gene.

Authors:  L Kao; J Krstenansky; J Mendell; K W Rammohan; E Gruenstein
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205
  4 in total

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