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Connection

Eden Haverfield to Sequence Analysis, DNA

This is a "connection" page, showing publications Eden Haverfield has written about Sequence Analysis, DNA.
Connection Strength

0.099
  1. Whole exome sequencing reveals de novo pathogenic variants in KAT6A as a cause of a neurodevelopmental disorder. Am J Med Genet A. 2016 07; 170(7):1791-8.
    View in: PubMed
    Score: 0.026
  2. Clinical application of whole-exome sequencing across clinical indications. Genet Med. 2016 07; 18(7):696-704.
    View in: PubMed
    Score: 0.026
  3. Mutations in DDX3X Are a Common Cause of Unexplained Intellectual Disability with Gender-Specific Effects on Wnt Signaling. Am J Hum Genet. 2015 Aug 06; 97(2):343-52.
    View in: PubMed
    Score: 0.025
  4. Molecular confirmation of nine cases of Cornelia de Lange syndrome diagnosed prenatally. Prenat Diagn. 2014 Feb; 34(2):163-7.
    View in: PubMed
    Score: 0.022
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.