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Q39127499-3D238EA9-1775-4039-9D16-DCD5B6912A1D
Q39127499-3D238EA9-1775-4039-9D16-DCD5B6912A1D
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http://www.wikidata.org/entity/statement/Q39127499-3D238EA9-1775-4039-9D16-DCD5B6912A1D
Chromosomal Microarrays: Understanding Genetics of Neurodevelopmental Disorders and Congenital Anomalies.
P2860
Q39127499-3D238EA9-1775-4039-9D16-DCD5B6912A1D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q39127499-3D238EA9-1775-4039-9D16-DCD5B6912A1D
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wasDerivedFrom
2ecf994bebacc2eb92a3a2a08d7ed9acf658fb42
P2860
Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome.