Literature DB >> 1338761

Insertion/deletion polymorphism at D19S95 associated with the myotonic dystrophy CTG repeat.

S R Crow1, H G Harley, J D Brook, S A Rundle, D J Shaw.   

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Year:  1992        PMID: 1338761     DOI: 10.1093/hmg/1.6.451

Source DB:  PubMed          Journal:  Hum Mol Genet        ISSN: 0964-6906            Impact factor:   6.150


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  3 in total

1.  Founder effect and prevalence of myotonic dystrophy in South Africans: molecular studies.

Authors:  A Goldman; A Krause; M Ramsay; T Jenkins
Journal:  Am J Hum Genet       Date:  1996-08       Impact factor: 11.025

2.  A study of DNA methylation in myotonic dystrophy.

Authors:  D J Shaw; S Chaudhary; S A Rundle; S Crow; J D Brook; P S Harper; H G Harley
Journal:  J Med Genet       Date:  1993-03       Impact factor: 6.318

3.  Triplet repeat expansion in myotonic dystrophy alters the adjacent chromatin structure.

Authors:  A D Otten; S J Tapscott
Journal:  Proc Natl Acad Sci U S A       Date:  1995-06-06       Impact factor: 11.205

  3 in total

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