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Connection

Eden Haverfield to Phenotype

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

0.190
  1. FTO variant associated with malformation syndrome. Am J Med Genet A. 2016 Apr; 170A(4):1023-8.
    View in: PubMed
    Score: 0.074
  2. 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: 0.072
  3. Cleft palate and hypopituitarism in a patient with Noonan-like syndrome with loose anagen hair-1. Am J Med Genet A. 2018 09; 176(9):2024-2027.
    View in: PubMed
    Score: 0.022
  4. Adaptation and validation of the ACMG/AMP variant classification framework for MYH7-associated inherited cardiomyopathies: recommendations by ClinGen's Inherited Cardiomyopathy Expert Panel. Genet Med. 2018 03; 20(3):351-359.
    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.