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Q46564552-CE75E600-BEF4-400D-B3EF-C8E2FD871A89
Q46564552-CE75E600-BEF4-400D-B3EF-C8E2FD871A89
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http://www.wikidata.org/entity/statement/Q46564552-CE75E600-BEF4-400D-B3EF-C8E2FD871A89
An infant with MLH3 variants, FOXG1-duplication and multiple, benign cranial and spinal tumors: A clinical exome sequencing study.
P2860
Q46564552-CE75E600-BEF4-400D-B3EF-C8E2FD871A89
BestRank
Statement
http://www.wikidata.org/entity/statement/Q46564552-CE75E600-BEF4-400D-B3EF-C8E2FD871A89
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wasDerivedFrom
91f591f956fc2d00a997f085d409eae4716c7481
P2860
Duplications of FOXG1 in 14q12 are associated with developmental epilepsy, mental retardation, and severe speech impairment.