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Q34629238-786998E3-A0AA-47DD-BCB2-31B566633D63
Q34629238-786998E3-A0AA-47DD-BCB2-31B566633D63
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Statement
http://www.wikidata.org/entity/statement/Q34629238-786998E3-A0AA-47DD-BCB2-31B566633D63
Microhomology-mediated mechanisms underlie non-recurrent disease-causing microdeletions of the FOXL2 gene or its regulatory domain.
P2860
Q34629238-786998E3-A0AA-47DD-BCB2-31B566633D63
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34629238-786998E3-A0AA-47DD-BCB2-31B566633D63
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wasDerivedFrom
fc215fd01f5536cd0ddf8ed6a6b1809039f12633
P2860
L1 recombination-associated deletions generate human genomic variation