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Q34629238-84D5234C-5BBF-4886-9CA4-F2AA02C02D0D
Q34629238-84D5234C-5BBF-4886-9CA4-F2AA02C02D0D
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Statement
http://www.wikidata.org/entity/statement/Q34629238-84D5234C-5BBF-4886-9CA4-F2AA02C02D0D
Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.
P2860
Q34629238-84D5234C-5BBF-4886-9CA4-F2AA02C02D0D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34629238-84D5234C-5BBF-4886-9CA4-F2AA02C02D0D
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wasDerivedFrom
fc215fd01f5536cd0ddf8ed6a6b1809039f12633
P2860
A microhomology-mediated break-induced replication model for the origin of human copy number variation.