Literature DB >> 1682892

A MseI polymorphism in exon 48 of the dystrophin gene.

S C Yau1, R G Roberts, D R Bentley, C G Mathew, M Bobrow.   

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Year:  1991        PMID： 1682892      PMCID： PMC329018          DOI： 10.1093/nar/19.20.5803-a

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


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  4 in total

1.  Primer-directed enzymatic amplification of DNA with a thermostable DNA polymerase.

Authors:  R K Saiki; D H Gelfand; S Stoffel; S J Scharf; R Higuchi; G T Horn; K B Mullis; H A Erlich
Journal:  Science       Date:  1988-01-29       Impact factor: 47.728

2.  Reactivity of cytosine and thymine in single-base-pair mismatches with hydroxylamine and osmium tetroxide and its application to the study of mutations.

Authors:  R G Cotton; N R Rodrigues; R D Campbell
Journal:  Proc Natl Acad Sci U S A       Date:  1988-06       Impact factor: 11.205

3.  Two human cDNA molecules coding for the Duchenne muscular dystrophy (DMD) locus are highly homologous.

Authors:  A Rosenthal; A Speer; H Billwitz; G S Cross; S M Forrest; K E Davies
Journal:  Nucleic Acids Res       Date:  1989-07-11       Impact factor: 16.971

4.  Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification.

Authors:  J S Chamberlain; R A Gibbs; J E Ranier; P N Nguyen; C T Caskey
Journal:  Nucleic Acids Res       Date:  1988-12-09       Impact factor: 16.971
  4 in total
  2 in total

1.  Point mutations in the dystrophin gene.

Authors:  R G Roberts; M Bobrow; D R Bentley
Journal:  Proc Natl Acad Sci U S A       Date:  1992-03-15       Impact factor: 11.205

2.  Microlesions and polymorphisms in the Duchenne/Becker muscular dystrophy gene.

Authors:  F Rininsland; J Reiss
Journal:  Hum Genet       Date:  1994-08       Impact factor: 4.132
  2 in total

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