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Q34388821-3B8A153F-73B3-4216-948B-866CB6F4683A
Q34388821-3B8A153F-73B3-4216-948B-866CB6F4683A
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http://www.wikidata.org/entity/statement/Q34388821-3B8A153F-73B3-4216-948B-866CB6F4683A
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome
P1433
Q34388821-3B8A153F-73B3-4216-948B-866CB6F4683A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34388821-3B8A153F-73B3-4216-948B-866CB6F4683A
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0ba4da4956d406b66c79711d246c53244617e480
P1433
American Journal of Human Genetics