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Genotype-phenotype correlation in 22q11.2 deletion syndrome.
Michaelovsky E, Frisch A, Carmel M, Patya M, Zarchi O, Green T, Basel-Vanagaite L, Weizman A, Gothelf D. Michaelovsky E, et al. Among authors: frisch a. BMC Med Genet. 2012 Dec 17;13:122. doi: 10.1186/1471-2350-13-122. BMC Med Genet. 2012. PMID: 23245648 Free PMC article.
Biological effects of COMT haplotypes and psychosis risk in 22q11.2 deletion syndrome.
Gothelf D, Law AJ, Frisch A, Chen J, Zarchi O, Michaelovsky E, Ren-Patterson R, Lipska BK, Carmel M, Kolachana B, Weizman A, Weinberger DR. Gothelf D, et al. Among authors: frisch a. Biol Psychiatry. 2014 Mar 1;75(5):406-13. doi: 10.1016/j.biopsych.2013.07.021. Epub 2013 Aug 28. Biol Psychiatry. 2014. PMID: 23992923 Free PMC article.
A comparative study of the neuropsychiatric and neurocognitive phenotype in two microdeletion syndromes: velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes.
Zarchi O, Diamond A, Weinberger R, Abbott D, Carmel M, Frisch A, Michaelovsky E, Gruber R, Green T, Weizman A, Gothelf D. Zarchi O, et al. Among authors: frisch a. Eur Psychiatry. 2014 May;29(4):203-10. doi: 10.1016/j.eurpsy.2013.07.001. Epub 2013 Sep 17. Eur Psychiatry. 2014. PMID: 24054518
299 results