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Q34478056-1B75DEC8-7DAF-496B-B0A3-0477D98A2059
Q34478056-1B75DEC8-7DAF-496B-B0A3-0477D98A2059
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34478056-1B75DEC8-7DAF-496B-B0A3-0477D98A2059
Dosage changes of a segment at 17p13.1 lead to intellectual disability and microcephaly as a result of complex genetic interaction of multiple genes.
P2860
Q34478056-1B75DEC8-7DAF-496B-B0A3-0477D98A2059
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34478056-1B75DEC8-7DAF-496B-B0A3-0477D98A2059
rank
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type
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Statement
wasDerivedFrom
27c84ccffe36a19085fcebbbb2d6fff5e396384b
P2860
Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.