Articles with "wdr4 mutations" as a keyword



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Speech and language delay in a patient with WDR4 mutations.

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Published in 2018 at "European journal of medical genetics"

DOI: 10.1016/j.ejmg.2018.03.007

Abstract: Primordial dwarfism (PD) is mainly characterized by growth deficiency with heterogeneous phenotypes. A group of genes are known to be associated with PD or PD-related syndrome. WD repeat domain 4 (WDR4) is recently reported to… read more here.

Keywords: language delay; speech language; wdr4; wdr4 mutations ... See more keywords