Publications

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Author Title [ Year(Desc)]
Filters: Keyword is Cranial Fontanelles  [Clear All Filters]
2014
Kaiser, F. J. et al. 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 23, 2888-900 (2014).