Eden Haverfield to Phenotype
This is a "connection" page, showing publications Eden Haverfield has written about Phenotype.
Connection Strength
0.190
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FTO variant associated with malformation syndrome. Am J Med Genet A. 2016 Apr; 170A(4):1023-8.
Score: 0.074
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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.
Score: 0.072
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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.
Score: 0.022
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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.
Score: 0.021