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Q38237562-E581E3F1-F1CA-4F37-9AD6-E10AA0DC06C9
Q38237562-E581E3F1-F1CA-4F37-9AD6-E10AA0DC06C9
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http://www.wikidata.org/entity/statement/Q38237562-E581E3F1-F1CA-4F37-9AD6-E10AA0DC06C9
Females with de novo aberrations in PHF6: clinical overlap of Borjeson-Forssman-Lehmann with Coffin-Siris syndrome.
P2860
Q38237562-E581E3F1-F1CA-4F37-9AD6-E10AA0DC06C9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38237562-E581E3F1-F1CA-4F37-9AD6-E10AA0DC06C9
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wasDerivedFrom
f1a5c249eb7d7ba1b381c75dcf5a8428a8ceb9af
P2860
Haploinsufficiency of ARID1B, a member of the SWI/SNF-a chromatin-remodeling complex, is a frequent cause of intellectual disability.