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Q35878239-0EF67154-3AD8-4263-B540-C7D8F18ED1E1
Q35878239-0EF67154-3AD8-4263-B540-C7D8F18ED1E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35878239-0EF67154-3AD8-4263-B540-C7D8F18ED1E1
High incidence of recurrent copy number variants in patients with isolated and syndromic Müllerian aplasia
P2860
Q35878239-0EF67154-3AD8-4263-B540-C7D8F18ED1E1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35878239-0EF67154-3AD8-4263-B540-C7D8F18ED1E1
rank
NormalRank
type
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Statement
wasDerivedFrom
5c19925031b578716c5c0dcf64070d7d9fb91e92
P2860
22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome.