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3. Risk of Psychiatric Disorders Among Individuals With the 22q11.2 Deletion or Duplication: A Danish Nationwide, Register-Based Study. Hoeffding LK; Trabjerg BB; Olsen L; Mazin W; Sparsø T; Vangkilde A; Mortensen PB; Pedersen CB; Werge T JAMA Psychiatry; 2017 Mar; 74(3):282-290. PubMed ID: 28114601 [TBL] [Abstract][Full Text] [Related]
4. [Microdeletion of 22q11, DiGeorge and velocardiofacial syndrome]. Hjalgrim H; Hahnemann JM; Timshel S; Brøndum-Nielsen K Ugeskr Laeger; 2000 Jul; 162(31):4169-70. PubMed ID: 10962926 [No Abstract] [Full Text] [Related]
5. Copy number variations and risk for schizophrenia in 22q11.2 deletion syndrome. Bassett AS; Marshall CR; Lionel AC; Chow EW; Scherer SW Hum Mol Genet; 2008 Dec; 17(24):4045-53. PubMed ID: 18806272 [TBL] [Abstract][Full Text] [Related]
6. [Phenotypic variability: genetics and chance--deletion 22q11 and schizophrenia]. Breuning MH Ned Tijdschr Geneeskd; 2002 Oct; 146(43):2016-9. PubMed ID: 12428459 [TBL] [Abstract][Full Text] [Related]
7. Is the autosomal dominant Optiz GBBB syndrome part of the DiGeorge/velocardiofacial syndrome with deletions of chromosome area 22q11.2? Wulfsberg EA Am J Med Genet; 1996 Aug; 64(3):523-4. PubMed ID: 8862634 [No Abstract] [Full Text] [Related]
9. The Top3β way to untangle RNA. Nott A; Tsai LH Nat Neurosci; 2013 Sep; 16(9):1163-4. PubMed ID: 23982446 [No Abstract] [Full Text] [Related]
10. Size of 22q deletions in four previously reported patients with conotruncal anomaly face syndrome. Pierpont JW; Erickson RP; Thompson FH; Yang JM Clin Genet; 1996 Dec; 50(6):545-7. PubMed ID: 9147896 [TBL] [Abstract][Full Text] [Related]
12. Schizophrenia with the 22q11.2 deletion and additional genetic defects: case history. Toyosima M; Maekawa M; Toyota T; Iwayama Y; Arai M; Ichikawa T; Miyashita M; Arinami T; Itokawa M; Yoshikawa T Br J Psychiatry; 2011 Sep; 199(3):245-6. PubMed ID: 21881099 [TBL] [Abstract][Full Text] [Related]
13. CATCH 22: deletion of locus 22q11 in velocardiofacial syndrome, DiGeorge anomaly, and nonsyndromic conotruncal defects. Hou JW; Wang JK; Tsai WY; Chou CC; Wang TR J Formos Med Assoc; 1997 Jun; 96(6):419-23. PubMed ID: 9216164 [TBL] [Abstract][Full Text] [Related]
15. The human mitochondrial citrate transporter gene (SLC20A3) maps to chromosome band 22q11 within a region implicated in DiGeorge syndrome, velo-cardio-facial syndrome and schizophrenia. Stoffel M; Karayiorgou M; Espinosa R; Beau MM Hum Genet; 1996 Jul; 98(1):113-5. PubMed ID: 8682495 [TBL] [Abstract][Full Text] [Related]
18. Positional mapping of loci in the DiGeorge critical region at chromosome 22q11 using a new marker (D22S183). Mulder MP; Wilke M; Langeveld A; Wilming LG; Hagemeijer A; van Drunen E; Zwarthoff EC; Riegman PH; Deelen WH; van den Ouweland AM Hum Genet; 1995 Aug; 96(2):133-41. PubMed ID: 7635459 [TBL] [Abstract][Full Text] [Related]
19. Genetic basis of DiGeorge and velocardiofacial syndromes. Driscoll DA Curr Opin Pediatr; 1994 Dec; 6(6):702-6. PubMed ID: 7849818 [TBL] [Abstract][Full Text] [Related]
20. Candidate genes and the behavioral phenotype in 22q11.2 deletion syndrome. Prasad SE; Howley S; Murphy KC Dev Disabil Res Rev; 2008; 14(1):26-34. PubMed ID: 18636634 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]