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Q33939049-AD560B57-DC2F-4A40-9A04-9D9478C49A69
Q33939049-AD560B57-DC2F-4A40-9A04-9D9478C49A69
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http://www.wikidata.org/entity/statement/Q33939049-AD560B57-DC2F-4A40-9A04-9D9478C49A69
Online Mendelian Inheritance in Man (OMIM) as a knowledgebase for human developmental disorders.
P2860
Q33939049-AD560B57-DC2F-4A40-9A04-9D9478C49A69
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33939049-AD560B57-DC2F-4A40-9A04-9D9478C49A69
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wasDerivedFrom
e3a348675f9fdb9dc6cf763e981f1cf0e5a0d843
P2860
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome