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Q33894385-F6888699-A1FD-4EA7-A4C8-C2343C30A7CC
Q33894385-F6888699-A1FD-4EA7-A4C8-C2343C30A7CC
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Statement
http://www.wikidata.org/entity/statement/Q33894385-F6888699-A1FD-4EA7-A4C8-C2343C30A7CC
Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1.
P2860
Q33894385-F6888699-A1FD-4EA7-A4C8-C2343C30A7CC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33894385-F6888699-A1FD-4EA7-A4C8-C2343C30A7CC
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wasDerivedFrom
672abd0b2ac55d57355b3df7134700df9f083aa4
P2860
Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes.