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Q24564244-5A6B35DD-4A6E-48FB-A3B5-75CF23A841BC
Q24564244-5A6B35DD-4A6E-48FB-A3B5-75CF23A841BC
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Statement
http://www.wikidata.org/entity/statement/Q24564244-5A6B35DD-4A6E-48FB-A3B5-75CF23A841BC
Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome
P2860
Q24564244-5A6B35DD-4A6E-48FB-A3B5-75CF23A841BC
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24564244-5A6B35DD-4A6E-48FB-A3B5-75CF23A841BC
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wasDerivedFrom
6a4efc51da639013a63e33fe53746448ffcdb5f4
P2860
Morphogenetic movements underlying eye field formation require interactions between the FGF and ephrinB1 signaling pathways.