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Human Molecular Genetics
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January 10, 2014
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance
Frank J Kaiser, Morad Ansari, Diana Braunholz, et al.
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Showing results (81-90 of 81) with videos related to
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Human Molecular Genetics
|
January 10, 2014
Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance
Frank J Kaiser, Morad Ansari, Diana Braunholz, et al.
Page
of 9