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Item type:Publication, Genetic contributors to risk of schizophrenia in the presence of a 22q11.2 deletion(2020) ;Isabelle Cleynen ;Worrawat Engchuan ;Matthew S. Hestand ;Tracy HeungAaron M. HollemanScopus© Citations 98 2 - Some of the metrics are blocked by yourconsent settings
Item type:Publication, Partial microduplication in the histone acetyltransferase complex member KANSL1 is associated with congenital heart defects in 22q11.2 microdeletion syndrome patients(2017) ;Luis E. León; ;Karena Espinoza ;Patricia Alvarez29 1Scopus© Citations 27