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11. A gender-moderated effect of a functional COMT polymorphism on prefrontal brain morphology and function in velo-cardio-facial syndrome (22q11.2 deletion syndrome). Kates WR, Antshel KM, Abdulsabur N, Colgan D, Funke B, Fremont W, Higgins AM, Kucherlapati R, Shprintzen RJ. Am J Med Genet B Neuropsychiatr Genet; 2006 Apr 05; 141B(3):274-80. PubMed ID: 16511839 [Abstract] [Full Text] [Related]
12. Schizophrenia and velo-cardio-facial syndrome. Murphy KC. Lancet; 2002 Feb 02; 359(9304):426-30. PubMed ID: 11844533 [Abstract] [Full Text] [Related]
13. Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia. Murphy KC, Owen MJ. Br J Psychiatry; 2001 Nov 02; 179():397-402. PubMed ID: 11689394 [Abstract] [Full Text] [Related]
14. Structural brain abnormalities associated with deletion at chromosome 22q11: quantitative neuroimaging study of adults with velo-cardio-facial syndrome. van Amelsvoort T, Daly E, Robertson D, Suckling J, Ng V, Critchley H, Owen MJ, Henry J, Murphy KC, Murphy DG. Br J Psychiatry; 2001 May 02; 178():412-9. PubMed ID: 11331556 [Abstract] [Full Text] [Related]
15. Velo-cardio-facial syndrome and psychotic disorders: implications for psychiatric genetics. Chow EW, Bassett AS, Weksberg R. Am J Med Genet; 1994 Jun 15; 54(2):107-12. PubMed ID: 8074160 [Abstract] [Full Text] [Related]
16. High rates of schizophrenia in adults with velo-cardio-facial syndrome. Murphy KC, Jones LA, Owen MJ. Arch Gen Psychiatry; 1999 Oct 15; 56(10):940-5. PubMed ID: 10530637 [Abstract] [Full Text] [Related]
17. Parental origin of the deletion 22q11.2 and brain development in velocardiofacial syndrome: a preliminary study. Eliez S, Antonarakis SE, Morris MA, Dahoun SP, Reiss AL. Arch Gen Psychiatry; 2001 Jan 15; 58(1):64-8. PubMed ID: 11146759 [Abstract] [Full Text] [Related]
18. [Congenital cardiovascular malformations and chromosome microdeletions in 22q11.2]. Trost D, Engels H, Bauriedel G, Wiebe W, Schwanitz G. Dtsch Med Wochenschr; 1999 Jan 08; 124(1-2):3-7. PubMed ID: 9951451 [Abstract] [Full Text] [Related]
19. Videonasopharyngoscopy in patients with 22q11.2 deletion syndrome (Shprintzen syndrome). Ysunza A, Pamplona MC, Ramírez E, Canún S, Sierra MC, Silva-Rojas A. Int J Pediatr Otorhinolaryngol; 2003 Aug 08; 67(8):911-5. PubMed ID: 12880672 [Abstract] [Full Text] [Related]
20. Confirmation that the velo-cardio-facial syndrome is associated with haplo-insufficiency of genes at chromosome 22q11. Kelly D, Goldberg R, Wilson D, Lindsay E, Carey A, Goodship J, Burn J, Cross I, Shprintzen RJ, Scambler PJ. Am J Med Genet; 1993 Feb 01; 45(3):308-12. PubMed ID: 8434616 [Abstract] [Full Text] [Related] Page: [Next] [New Search]