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Q55362263-A9C710AD-5A47-49DB-BD1D-D5ECD70CF37B
Q55362263-A9C710AD-5A47-49DB-BD1D-D5ECD70CF37B
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http://www.wikidata.org/entity/statement/Q55362263-A9C710AD-5A47-49DB-BD1D-D5ECD70CF37B
Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.
P2860
Q55362263-A9C710AD-5A47-49DB-BD1D-D5ECD70CF37B
BestRank
Statement
http://www.wikidata.org/entity/statement/Q55362263-A9C710AD-5A47-49DB-BD1D-D5ECD70CF37B
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wasDerivedFrom
ac5bdebbbd5095b7d1915682ee3ee2305798b321
P2860
Functional analysis of candidate genes in 2q13 deletion syndrome implicates FBLN7 and TMEM87B deficiency in congenital heart defects and FBLN7 in craniofacial malformations.