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Q34629238-6E45DB45-6F73-4A8D-AABD-AA12F3D81BB5
Q34629238-6E45DB45-6F73-4A8D-AABD-AA12F3D81BB5
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Statement
http://www.wikidata.org/entity/statement/Q34629238-6E45DB45-6F73-4A8D-AABD-AA12F3D81BB5
Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.
P2860
Q34629238-6E45DB45-6F73-4A8D-AABD-AA12F3D81BB5
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34629238-6E45DB45-6F73-4A8D-AABD-AA12F3D81BB5
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wasDerivedFrom
fc215fd01f5536cd0ddf8ed6a6b1809039f12633
P2860
Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening.