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Q37011287-A47D2DFF-ABAE-42CB-9292-BCB38AA5E6E0
Q37011287-A47D2DFF-ABAE-42CB-9292-BCB38AA5E6E0
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Statement
http://www.wikidata.org/entity/statement/Q37011287-A47D2DFF-ABAE-42CB-9292-BCB38AA5E6E0
Cytogenetic and array-CGH characterization of a complex de novo rearrangement involving duplication and deletion of 9p and clinical findings in a 4-month-old female.
P2860
Q37011287-A47D2DFF-ABAE-42CB-9292-BCB38AA5E6E0
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37011287-A47D2DFF-ABAE-42CB-9292-BCB38AA5E6E0
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type
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wasDerivedFrom
3883f6ca0cc7d0985412808f5ea1be7363370270
P2860
Impaired male sex development in an infant with molecularly defined partial 9p monosomy: implication for a testis forming gene(s) on 9p.