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Q36809678-0930A8EE-98BB-4150-9724-BE2232E850E9
Q36809678-0930A8EE-98BB-4150-9724-BE2232E850E9
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http://www.wikidata.org/entity/statement/Q36809678-0930A8EE-98BB-4150-9724-BE2232E850E9
14q12 microdeletions excluding FOXG1 give rise to a congenital variant Rett syndrome-like phenotype.
P2860
Q36809678-0930A8EE-98BB-4150-9724-BE2232E850E9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36809678-0930A8EE-98BB-4150-9724-BE2232E850E9
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fb4ac4a9bbc6c98804199e86d49768ff5f4e29fd
P2860
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.