Literature DB >> 3016653

RFLPs at the D19S19 locus of human chromosome 19 linked to myotonic dystrophy (DM).

A D Roses, M A Pericak-Vance, D A Ross, L Yamaoka, R J Bartlett.   

Abstract

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Year:  1986        PMID： 3016653      PMCID： PMC311567          DOI： 10.1093/nar/14.13.5569

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


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  5 in total

1.  Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q.

Authors:  K Johnson; E Nimmo; P Jones; M Weiss; M L Savontaus; M Anvret; R Bartlett; A Roses; D Shaw; P S Harper
Journal:  Hum Genet       Date:  1988-12       Impact factor: 4.132

Review 2.  Diagnosis of genetic disease using recombinant DNA. Supplement.

Authors:  D N Cooper; J Schmidtke
Journal:  Hum Genet       Date:  1987-09       Impact factor: 4.132

3.  Exclusion of the Friedreich ataxia gene from chromosome 19.

Authors:  S Chamberlain; C S Worrall; S South; J Shaw; M Farrall; R Williamson
Journal:  Hum Genet       Date:  1987-06       Impact factor: 4.132

4.  Three-point linkage analysis employing C3 and 19cen markers assigns the myotonic dystrophy gene to 19q.

Authors:  U Friedrich; H Brunner; D Smeets; E Lambermon; H H Ropers
Journal:  Hum Genet       Date:  1987-03       Impact factor: 4.132

5.  Application of a closely linked polymorphism of restriction fragment length to counselling and prenatal testing in families with myotonic dystrophy.

Authors:  A L Meredith; S M Huson; P W Lunt; M Sarfarazi; H G Harley; J D Brook; D J Shaw; P S Harper
Journal:  Br Med J (Clin Res Ed)       Date:  1986-11-22
  5 in total

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