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Q26784240-4F709737-369E-412A-8CDA-8E7985E0F22A
Q26784240-4F709737-369E-412A-8CDA-8E7985E0F22A
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http://www.wikidata.org/entity/statement/Q26784240-4F709737-369E-412A-8CDA-8E7985E0F22A
A Genetic-Pathophysiological Framework for Craniosynostosis
P2860
Q26784240-4F709737-369E-412A-8CDA-8E7985E0F22A
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http://www.wikidata.org/entity/statement/Q26784240-4F709737-369E-412A-8CDA-8E7985E0F22A
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wasDerivedFrom
ffd2aa53a51c3f920fc6231ff939a6dc9142e64f
P2860
De novo alu-element insertions in FGFR2 identify a distinct pathological basis for Apert syndrome