Connection

JULIE GASTIER-FOSTER to Exons

This is a "connection" page, showing publications JULIE GASTIER-FOSTER has written about Exons.
Connection Strength

0.198
  1. Exonic deletions in AUTS2 cause a syndromic form of intellectual disability and suggest a critical role for the C terminus. Am J Hum Genet. 2013 Feb 07; 92(2):210-20.
    View in: PubMed
    Score: 0.081
  2. Evolutionary relationships among Rel domains indicate functional diversification by recombination. Proc Natl Acad Sci U S A. 2001 May 08; 98(10):5740-5.
    View in: PubMed
    Score: 0.036
  3. Diverse deletions in the growth hormone receptor gene cause growth hormone insensitivity syndrome. Hum Mutat. 2000 Oct; 16(4):323-33.
    View in: PubMed
    Score: 0.035
  4. MCPH1 deletion in a newborn with severe microcephaly and premature chromosome condensation. Eur J Med Genet. 2013 Nov; 56(11):609-13.
    View in: PubMed
    Score: 0.021
  5. Contactin 4 as an autism susceptibility locus. Autism Res. 2011 Jun; 4(3):189-99.
    View in: PubMed
    Score: 0.018
  6. Novel mutations in the Wiskott-Aldrich syndrome protein gene and their effects on transcriptional, translational, and clinical phenotypes. Hum Mutat. 1999; 14(1):54-66.
    View in: PubMed
    Score: 0.008
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.