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Q24564244-0167BECD-6249-4175-BF04-79AD73DAA3F2
Q24564244-0167BECD-6249-4175-BF04-79AD73DAA3F2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24564244-0167BECD-6249-4175-BF04-79AD73DAA3F2
Mutations of ephrin-B1 (EFNB1), a marker of tissue boundary formation, cause craniofrontonasal syndrome
P2860
Q24564244-0167BECD-6249-4175-BF04-79AD73DAA3F2
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24564244-0167BECD-6249-4175-BF04-79AD73DAA3F2
rank
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type
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Statement
wasDerivedFrom
68002986ccfeeb89324a82b030237b91ff71d7f7
P2860
Skewed X-chromosome inactivation is a common feature of X-linked mental retardation disorders.