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1
6419c1531b88a3f5ac69fcba3a1721a352bfb566
6419c1531b88a3f5ac69fcba3a1721a352bfb566
Reference
http://www.wikidata.org/reference/6419c1531b88a3f5ac69fcba3a1721a352bfb566
Q55784939-264F1A46-8734-438B-A209-2948AC83C686
Q55784939-43FB848F-69C0-4321-8544-29C966A5C218
wasDerivedFrom
6419c1531b88a3f5ac69fcba3a1721a352bfb566
Reference
http://www.wikidata.org/reference/6419c1531b88a3f5ac69fcba3a1721a352bfb566
type
Reference
P248
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.