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Q24673460-368F48A7-4900-42AD-A0BF-2D69C9EFABB2
Q24673460-368F48A7-4900-42AD-A0BF-2D69C9EFABB2
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http://www.wikidata.org/entity/statement/Q24673460-368F48A7-4900-42AD-A0BF-2D69C9EFABB2
Mutational analyses of UPIIIA, SHH, EFNB2 and HNF1beta in persistent cloaca and associated kidney malformations
P2860
Q24673460-368F48A7-4900-42AD-A0BF-2D69C9EFABB2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24673460-368F48A7-4900-42AD-A0BF-2D69C9EFABB2
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wasDerivedFrom
b974736a1b49b05cf9ff01b0ef98f00b7f7d9cd0
P2860
Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome