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Q34238113-3BFF3252-2EDE-4D35-B5B6-3EFDD435B596
Q34238113-3BFF3252-2EDE-4D35-B5B6-3EFDD435B596
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Statement
http://www.wikidata.org/entity/statement/Q34238113-3BFF3252-2EDE-4D35-B5B6-3EFDD435B596
The clinical significance of small copy number variants in neurodevelopmental disorders
P2860
Q34238113-3BFF3252-2EDE-4D35-B5B6-3EFDD435B596
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34238113-3BFF3252-2EDE-4D35-B5B6-3EFDD435B596
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wasDerivedFrom
cc2e3145666f9fb4bef8cf2fd365050243c6369e
P2860
Range of genetic mutations associated with severe non-syndromic sporadic intellectual disability: an exome sequencing study