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Vorstman, Jacob A. S.; Breetvelt, Elemi J.; Thode, Kirstin I.; Chow, Eva W. C.; Bassett, Anne S. (xaneiro de 2013). "Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion". Schizophrenia Research143 (1): 55–59. ISSN1573-2509. PMID23153825. doi:10.1016/j.schres.2012.10.010.
Vorstman, Jacob A.S.; Breetvelt, Elemi J.; Thode, Kirstin I.; Chow, Eva W.C.; Bassett, Anne S. (xaneiro de 2013). "Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion". Schizophrenia Research143 (1): 55–59. PMID23153825. doi:10.1016/j.schres.2012.10.010.
Sullivan, Patrick F.; Kendler, Kenneth S.; Neale, Michael C. (2003-12-01). "Schizophrenia as a complex trait: evidence from a meta-analysis of twin studies". Archives of General Psychiatry60 (12): 1187–1192. PMID14662550. doi:10.1001/archpsyc.60.12.1187.
Forrest, Iain S.; Chaudhary, Kumardeep; Vy, Ha My T.; Bafna, Shantanu; Kim, Soyeon; Won, Hong-Hee; Loos, Ruth J. F.; Cho, Judy; Pasquale, Louis R.; Nadkarni, Girish N.; Rocheleau, Ghislain (2021). "Genetic pleiotropy of ERCC6 loss-of-function and deleterious missense variants links retinal dystrophy, arrhythmia, and immunodeficiency in diverse ancestries". Human Mutation(en inglés)n/a (n/a). ISSN1098-1004. PMID34005834. doi:10.1002/humu.24220.
Vorstman, Jacob A. S.; Breetvelt, Elemi J.; Thode, Kirstin I.; Chow, Eva W. C.; Bassett, Anne S. (xaneiro de 2013). "Expression of autism spectrum and schizophrenia in patients with a 22q11.2 deletion". Schizophrenia Research143 (1): 55–59. ISSN1573-2509. PMID23153825. doi:10.1016/j.schres.2012.10.010.
Forrest, Iain S.; Chaudhary, Kumardeep; Vy, Ha My T.; Bafna, Shantanu; Kim, Soyeon; Won, Hong-Hee; Loos, Ruth J. F.; Cho, Judy; Pasquale, Louis R.; Nadkarni, Girish N.; Rocheleau, Ghislain (2021). "Genetic pleiotropy of ERCC6 loss-of-function and deleterious missense variants links retinal dystrophy, arrhythmia, and immunodeficiency in diverse ancestries". Human Mutation(en inglés)n/a (n/a). ISSN1098-1004. PMID34005834. doi:10.1002/humu.24220.