Journal

Human Molecular Genetics

ISSN 0964-6906 · Oxford University Press

OpenAlex S166515463

Published here

1 counted work of 1 linked

YearTitleAcademicsSources
2014 Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked … David W. Christianson GS