Connection

PAWEL STANKIEWICZ to Chromosomes, Human, Pair 20

This is a "connection" page, showing publications PAWEL STANKIEWICZ has written about Chromosomes, Human, Pair 20.
  1. Alagille syndrome associated with a paracentric inversion 20p12.2p13 disrupting the JAG1 gene. Am J Med Genet. 2001 Oct 01; 103(2):166-71.
    View in: PubMed
    Score: 0.176
  2. SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delay. Am J Med Genet B Neuropsychiatr Genet. 2013 Dec; 162B(8):832-40.
    View in: PubMed
    Score: 0.101
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.