Connection

IRENE NEWSHAM to Craniofacial Abnormalities

This is a "connection" page, showing publications IRENE NEWSHAM has written about Craniofacial Abnormalities.
Connection Strength

0.021
  1. Whole-exome sequencing identifies compound heterozygous mutations in WDR62 in siblings with recurrent polymicrogyria. Am J Med Genet A. 2011 Sep; 155A(9):2071-7.
    View in: PubMed
    Score: 0.021
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.