GeneMatcher Aids in the Identification of a New Malformation Syndrome with Intellectual Disability, Unique Facial Dysmorphisms, and Skeletal and Connective Tissue Abnormalities Caused by De Novo Variants in HNRNPK

Publisher： John Wiley & Sons Inc

E-ISSN： 1098-1004|1059-7794|10|1009-1014

ISSN： 1059-7794

Source： HUMAN MUTATION, Vol.1059-7794, Iss.10, 2015-10, pp. : 1009-1014

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