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