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Q35223619-BD75F33D-C4F3-465D-BA6B-D1F92996F56B
Q35223619-BD75F33D-C4F3-465D-BA6B-D1F92996F56B
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Statement
http://www.wikidata.org/entity/statement/Q35223619-BD75F33D-C4F3-465D-BA6B-D1F92996F56B
Phenotypic and genetic characterization of a family carrying two Xq21.1-21.3 interstitial deletions associated with syndromic hearing loss.
P2860
Q35223619-BD75F33D-C4F3-465D-BA6B-D1F92996F56B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q35223619-BD75F33D-C4F3-465D-BA6B-D1F92996F56B
rank
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type
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Statement
wasDerivedFrom
ae734a49391ed59eed17e854014eaf003526a3a3
P2860
Choroideremia and deafness with stapes fixation: a contiguous gene deletion syndrome in Xq21