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Q33894385-F71417B2-36F8-45FB-90ED-320D9E7A4E68
Q33894385-F71417B2-36F8-45FB-90ED-320D9E7A4E68
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http://www.wikidata.org/entity/statement/Q33894385-F71417B2-36F8-45FB-90ED-320D9E7A4E68
Phenotypes of craniofrontonasal syndrome in patients with a pathogenic mutation in EFNB1.
P2860
Q33894385-F71417B2-36F8-45FB-90ED-320D9E7A4E68
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33894385-F71417B2-36F8-45FB-90ED-320D9E7A4E68
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wasDerivedFrom
672abd0b2ac55d57355b3df7134700df9f083aa4
P2860
Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome