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Project Title
Genetic modifiers of the cardiovascular phenotype of chromosome 22q11 micro deletion syndrome: Next-generation sequencing of candidate regions identified by genome-wide association analysis
Partner Organisations
Internal ID
1130392
Principal Investigator
Status
TERMINADO
Start Date
2013
Keywords
Views
6
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Acquisition Date
Nov 21, 2024
Nov 21, 2024
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PublicationVariance of IQ is partially dependent on deletion type among 1,427 22q11.2 deletion syndrome subjects( 2018)
Scopus© Citations 30 12 -
Publication
Scopus© Citations 25 14 -
PublicationNeuroimaging and clinical features in adults with a 22q11.2 deletion at risk of Parkinson’s disease( 2017)
Scopus© Citations 41 13