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Q52776190-8C7D111E-61F7-4821-9F87-3395CE61FEDF
Q52776190-8C7D111E-61F7-4821-9F87-3395CE61FEDF
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Statement
http://www.wikidata.org/entity/statement/Q52776190-8C7D111E-61F7-4821-9F87-3395CE61FEDF
Marked yield of re-evaluating phenotype and exome/target sequencing data in 33 individuals with intellectual disabilities.
P2860
Q52776190-8C7D111E-61F7-4821-9F87-3395CE61FEDF
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52776190-8C7D111E-61F7-4821-9F87-3395CE61FEDF
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wasDerivedFrom
5dfca0dc88ca6b26dcea9f4ca774035ef1dadfd9
P2860
Mutations in MED12 cause X-linked Ohdo syndrome