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Q58611455-E67F58B8-BEC9-46A4-980F-022E9F2F41A7
Q58611455-E67F58B8-BEC9-46A4-980F-022E9F2F41A7
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http://www.wikidata.org/entity/statement/Q58611455-E67F58B8-BEC9-46A4-980F-022E9F2F41A7
CHD3 helicase domain mutations cause a neurodevelopmental syndrome with macrocephaly and impaired speech and language
P2860
Q58611455-E67F58B8-BEC9-46A4-980F-022E9F2F41A7
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58611455-E67F58B8-BEC9-46A4-980F-022E9F2F41A7
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ef92bcb8cc81c4d4a95aca1c1a8e4f71d85f1dc0
P2860
Distinct genetic architectures for syndromic and nonsyndromic congenital heart defects identified by exome sequencing.