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Q55982492-B8A04A0F-568F-4C26-8673-3B7A56F23D99
Q55982492-B8A04A0F-568F-4C26-8673-3B7A56F23D99
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Statement
http://www.wikidata.org/entity/statement/Q55982492-B8A04A0F-568F-4C26-8673-3B7A56F23D99
Delineation of clinical features in Wiedemann-Steiner syndrome caused by KMT2A mutations
P2860
Q55982492-B8A04A0F-568F-4C26-8673-3B7A56F23D99
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55982492-B8A04A0F-568F-4C26-8673-3B7A56F23D99
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wasDerivedFrom
8a13fa376a322d2535f218f739482e211077df06
P2860
De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing.