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Q28586812-9F2B6D05-6550-49A5-97F6-A2EE0178BA0E
Q28586812-9F2B6D05-6550-49A5-97F6-A2EE0178BA0E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28586812-9F2B6D05-6550-49A5-97F6-A2EE0178BA0E
YY1 activates Msx2 gene independent of bone morphogenetic protein signaling.
P2860
Q28586812-9F2B6D05-6550-49A5-97F6-A2EE0178BA0E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q28586812-9F2B6D05-6550-49A5-97F6-A2EE0178BA0E
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Statement
wasDerivedFrom
d33fdf35f3a8669edfa96fb22193fb634e985f34
P2860
A mutation in the homeodomain of the human MSX2 gene in a family affected with autosomal dominant craniosynostosis