Literature DB >> 2020555

A dinucleotide repeat polymorphism at the DMD locus.

J F Powell1, F H Fodor, D J Cockburn, A P Monaco, I W Craig.   

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Year:  1991        PMID： 2020555      PMCID： PMC333808          DOI： 10.1093/nar/19.5.1159-a

Source DB:  PubMed          Journal:  Nucleic Acids Res        ISSN： 0305-1048            Impact factor:   16.971


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  1 in total

1.  Complete cloning of the Duchenne muscular dystrophy (DMD) cDNA and preliminary genomic organization of the DMD gene in normal and affected individuals.

Authors:  M Koenig; E P Hoffman; C J Bertelson; A P Monaco; C Feener; L M Kunkel
Journal:  Cell       Date:  1987-07-31       Impact factor: 41.582
  1 in total
  4 in total

1.  Informative microsatellite markers allow carrier detection in a Duchenne muscular dystrophy deletion pedigree in the absence of DNA from an affected boy.

Authors:  R I Richards; K Friend; E A Haan
Journal:  Am J Hum Genet       Date:  1992-02       Impact factor: 11.025

2.  Spectrum of small mutations in the dystrophin coding region.

Authors:  T W Prior; C Bartolo; D K Pearl; A C Papp; P J Snyder; M S Sedra; A H Burghes; J R Mendell
Journal:  Am J Hum Genet       Date:  1995-07       Impact factor: 11.025

3.  Determination of Duchenne muscular dystrophy carrier status by single strand conformation polymorphism analysis of deleted regions of the dystrophin locus.

Authors:  R I Richards; K Friend
Journal:  J Med Genet       Date:  1991-12       Impact factor: 6.318

Review 4.  Dilated cardiomyopathy and the dystrophin gene: an illustrated review.

Authors:  A Oldfors; B O Eriksson; M Kyllerman; T Martinsson; J Wahlström
Journal:  Br Heart J       Date:  1994-10
  4 in total

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