Connection

FERNANDO SCAGLIA to Karyotyping

This is a "connection" page, showing publications FERNANDO SCAGLIA has written about Karyotyping.
Connection Strength

0.090
  1. The Xp contiguous deletion syndrome and autism. Am J Med Genet A. 2009 Jun; 149A(6):1138-48.
    View in: PubMed
    Score: 0.072
  2. Chromosome 8p23.1 deletions as a cause of complex congenital heart defects and diaphragmatic hernia. Am J Med Genet A. 2009 Aug; 149A(8):1661-77.
    View in: PubMed
    Score: 0.018
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.