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Q28591998-E3DFF66A-560D-473E-B543-7F099641030B
Q28591998-E3DFF66A-560D-473E-B543-7F099641030B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28591998-E3DFF66A-560D-473E-B543-7F099641030B
Msx1 disruption leads to diencephalon defects and hydrocephalus
P2860
Q28591998-E3DFF66A-560D-473E-B543-7F099641030B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28591998-E3DFF66A-560D-473E-B543-7F099641030B
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wasDerivedFrom
29b72f1e8ab9939841529348eae1b9e5fcf8883d
P2860
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis