Connection

RICHARD GIBBS to Muscular Dystrophies

This is a "connection" page, showing publications RICHARD GIBBS has written about Muscular Dystrophies.
Connection Strength

0.098
  1. Accurate determination of DNA in agarose gels using the novel algorithm GelScann(1.0). Comput Appl Biosci. 1995 Apr; 11(2):187-94.
    View in: PubMed
    Score: 0.028
  2. Identification of a 2 base pair nonsense mutation causing a cryptic splice site in a DMD patient. Hum Mol Genet. 1992 Nov; 1(8):645-6.
    View in: PubMed
    Score: 0.024
  3. Carrier detection and prenatal diagnosis in Duchenne and Becker muscular dystrophy families, using dinucleotide repeat polymorphisms. Am J Hum Genet. 1991 Nov; 49(5):951-60.
    View in: PubMed
    Score: 0.022
  4. Deletion screening of the Duchenne muscular dystrophy locus via multiplex DNA amplification. Nucleic Acids Res. 1988 Dec 09; 16(23):11141-56.
    View in: PubMed
    Score: 0.018
  5. A transposon-like element in the deletion-prone region of the dystrophin gene. Genomics. 1992 Jul; 13(3):594-600.
    View in: PubMed
    Score: 0.006
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.