ELIZABETH ROEDER to Hypertelorism
This is a "connection" page, showing publications ELIZABETH ROEDER has written about Hypertelorism.
Connection Strength
0.116
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Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance. Hum Mol Genet. 2014 Jun 01; 23(11):2888-900.
Score: 0.116