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Q52861892-81113A41-509F-45B4-AEDD-EF897304A6C8
Q52861892-81113A41-509F-45B4-AEDD-EF897304A6C8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52861892-81113A41-509F-45B4-AEDD-EF897304A6C8
On the significance of craniosynostosis in a case of Kabuki syndrome with a concomitant KMT2D mutation and 3.2 Mbp de novo 10q22.3q23.1 deletion.
P2860
Q52861892-81113A41-509F-45B4-AEDD-EF897304A6C8
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52861892-81113A41-509F-45B4-AEDD-EF897304A6C8
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type
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Statement
wasDerivedFrom
8cbd4fe6309bcd98725ea9db0f47a9fcb944da3c
P2860
The phenotype of recurrent 10q22q23 deletions and duplications.