A novel mutation of orthodenticle homeobox 2 contributing to a case of otocephaly initially diagnosed by prenatal ultrasound in the first trimester.

Meredith Jones Judith Chung Virginia Kimonis June-Anne Gold

Clin Dysmorphol

aDepartment of Pediatrics, Division of Genetic and Genomic Medicine bDepartment of Obstetrics and Gynecology, University of California Irvine, Orange cDepartment of Pediatrics, Loma Linda University Health, Loma Linda, California, USA.

Published: April 2017

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http://dx.doi.org/10.1097/MCD.0000000000000145	DOI Listing

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