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Q24604419-A669BBA5-475B-4EBC-98D8-5D970330910D
Q24604419-A669BBA5-475B-4EBC-98D8-5D970330910D
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Statement
http://www.wikidata.org/entity/statement/Q24604419-A669BBA5-475B-4EBC-98D8-5D970330910D
Childhood Apraxia of Speech (CAS) in two patients with 16p11.2 microdeletion syndrome.
P2860
Q24604419-A669BBA5-475B-4EBC-98D8-5D970330910D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24604419-A669BBA5-475B-4EBC-98D8-5D970330910D
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type
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wasDerivedFrom
22bd9154a9eef4a83f0ba297725ac8236ca04284
P2860
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.