%0 Journal Article
%T Risk gene-set and pathways in 22q11.2 deletion-related schizophrenia: a genealogical molecular approach
%A Abraham Weizman
%A Amos Frisch
%A Doron Gothelf
%A Elena Michaelovsky
%A Mali Salmon-Divon
%A Metsada Pasmanik-Chor
%A Miri Carmel
%J Archive of "Translational Psychiatry".
%D 2019
%R 10.1038/s41398-018-0354-9
%X The analysis process designed for identifying molecular variants that may contribute to SZ-spectrum disorders in a multiplex 22q11.2DS family. Filled symbols indicate 22q11.2DS affected person with the same 22q11.2 deletion (CGH-array: chr22:18,844,632-21,703,145, GRCh37). *No DNA was available for these family members. BPE brief psychotic episode, CGH comparative-genomic hybridization, CNV copy number variation, DD delusional disorder, MLPA multiplex ligation probe amplification, SZ schizophreni
%U https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6358611/