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Q34388821-0DC46CE1-B0C7-4AFB-BF98-0CDB6311964A
Q34388821-0DC46CE1-B0C7-4AFB-BF98-0CDB6311964A
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http://www.wikidata.org/entity/statement/Q34388821-0DC46CE1-B0C7-4AFB-BF98-0CDB6311964A
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome
P2860
Q34388821-0DC46CE1-B0C7-4AFB-BF98-0CDB6311964A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34388821-0DC46CE1-B0C7-4AFB-BF98-0CDB6311964A
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wasDerivedFrom
816aedeaa36f84fc07f2d94649bfae212acef35b
P2860
Apert syndrome. Classification and pathologic anatomy of limb anomalies.