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Connection

Marion Verp to Prader-Willi Syndrome

This is a "connection" page, showing publications Marion Verp has written about Prader-Willi Syndrome.
Connection Strength

0.070
  1. Analysis of parent of origin specific DNA methylation at SNRPN and PW71 in tissues: implication for prenatal diagnosis. J Med Genet. 1996 Dec; 33(12):1011-4.
    View in: PubMed
    Score: 0.036
  2. Prenatal diagnosis of uniparental disomy 15 following trisomy 15 mosaicism. Prenat Diagn. 1996 Apr; 16(4):323-32.
    View in: PubMed
    Score: 0.034
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.