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Q37640927-449D2714-29C2-45EC-B69D-E4A42F5ADAA9
Q37640927-449D2714-29C2-45EC-B69D-E4A42F5ADAA9
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http://www.wikidata.org/entity/statement/Q37640927-449D2714-29C2-45EC-B69D-E4A42F5ADAA9
The genomic landscape of balanced cytogenetic abnormalities associated with human congenital anomalies.
P2860
Q37640927-449D2714-29C2-45EC-B69D-E4A42F5ADAA9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37640927-449D2714-29C2-45EC-B69D-E4A42F5ADAA9
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type
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wasDerivedFrom
050abc101615450fcb5b0802f893073a2a579839
P2860
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.