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Q34323553-5D4C566F-9306-424E-A91D-107DD53A70F7
Q34323553-5D4C566F-9306-424E-A91D-107DD53A70F7
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Statement
http://www.wikidata.org/entity/statement/Q34323553-5D4C566F-9306-424E-A91D-107DD53A70F7
Cellular interference in craniofrontonasal syndrome: males mosaic for mutations in the X-linked EFNB1 gene are more severely affected than true hemizygotes.
P2860
Q34323553-5D4C566F-9306-424E-A91D-107DD53A70F7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34323553-5D4C566F-9306-424E-A91D-107DD53A70F7
rank
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type
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wasDerivedFrom
505a15deaabbc13cdea8469762aff462dbd8fba5
P2860
Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome