Jacquelyn J. Bradley

Internal Medicine

150 Bergen St # H-245
Newark, NJ 07103

Last Updated: 09/26/2026

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Found 1 publications

Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance.

Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance.

Journal: Human molecular genetics

Published: January 10, 2014

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Last Updated: 09/26/2026