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Q34702033-59EB273A-C407-4564-8F1E-3E154EEB9204
Q34702033-59EB273A-C407-4564-8F1E-3E154EEB9204
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http://www.wikidata.org/entity/statement/Q34702033-59EB273A-C407-4564-8F1E-3E154EEB9204
Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome.
P2860
Q34702033-59EB273A-C407-4564-8F1E-3E154EEB9204
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34702033-59EB273A-C407-4564-8F1E-3E154EEB9204
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wasDerivedFrom
5e084ff8c79fcfbe84edee891c04a7647e6dc963
P2860
Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome