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22. DiGeorge syndrome: clinical variability in a family with submicroscopic deletion at 22q11.2. Tsui KM; Ng YY; Lam TS Zhonghua Min Guo Xiao Er Ke Yi Xue Hui Za Zhi; 1997; 38(1):52-6. PubMed ID: 9066191 [TBL] [Abstract][Full Text] [Related]
23. Breakpoint Associated with a novel 2.3 Mb deletion in the VCFS region of 22q11 and the role of Alu (SINE) in recurring microdeletions. Uddin RK; Zhang Y; Siu VM; Fan YS; O'Reilly RL; Rao J; Singh SM BMC Med Genet; 2006 Mar; 7():18. PubMed ID: 16512914 [TBL] [Abstract][Full Text] [Related]
24. [Clinical heterogeneity of the chromosome 22q11 microdeletion syndrome]. Muñoz S; Garay F; Flores I; Heusser F; Talesnik E; Aracena M; Mellado C; Méndez C; Arnaiz P; Repetto G Rev Med Chil; 2001 May; 129(5):515-21. PubMed ID: 11464533 [TBL] [Abstract][Full Text] [Related]
25. [Partial DiGeorge syndrome caused by 22q11.2 typical microdeletion without cardiac defect: report of two cases]. He JX; Zhang S; Han TL; Yu FH; Liu XY; Xu BP; Shen KL; Jiang ZF Zhongguo Dang Dai Er Ke Za Zhi; 2014 May; 16(5):541-3. PubMed ID: 24857009 [No Abstract] [Full Text] [Related]
27. Developmental presentation of 22q11.2 deletion (DiGeorge/velocardiofacial syndrome). Wang PP; Solot C; Moss EM; Gerdes M; McDonald-McGinn DM; Driscoll DA; Emanuel BS; Zackai EH J Dev Behav Pediatr; 1998 Oct; 19(5):342-5. PubMed ID: 9809264 [No Abstract] [Full Text] [Related]
28. Labyrinthine malformation in the 22q11.2 deletion syndrome. Hopsu E; Markkola A; Pitkäranta A Clin Dysmorphol; 2007 Jan; 16(1):67-68. PubMed ID: 17159521 [TBL] [Abstract][Full Text] [Related]
29. Genes, brain development and psychiatric phenotypes in velo-cardio-facial syndrome. Gothelf D; Schaer M; Eliez S Dev Disabil Res Rev; 2008; 14(1):59-68. PubMed ID: 18636637 [TBL] [Abstract][Full Text] [Related]
30. Allergies in patients with chromosome 22q11.2 deletion syndrome (DiGeorge syndrome/velocardiofacial syndrome) and patients with chronic granulomatous disease. Staple L; Andrews T; McDonald-McGinn D; Zackai E; Sullivan KE Pediatr Allergy Immunol; 2005 May; 16(3):226-30. PubMed ID: 15853951 [TBL] [Abstract][Full Text] [Related]
31. 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]
32. DiGeorge syndrome: new insights. Goldmuntz E Clin Perinatol; 2005 Dec; 32(4):963-78, ix-x. PubMed ID: 16325672 [TBL] [Abstract][Full Text] [Related]
33. A novel 22q11.2 microdeletion in DiGeorge syndrome. Rauch A; Pfeiffer RA; Leipold G; Singer H; Tigges M; Hofbeck M Am J Hum Genet; 1999 Feb; 64(2):659-66. PubMed ID: 9973528 [No Abstract] [Full Text] [Related]
34. Cognitive behavioral therapy in 22q11.2 microdeletion with psychotic symptoms: What do we learn from schizophrenia? Demily C; Franck N Eur J Med Genet; 2016 Nov; 59(11):596-603. PubMed ID: 27639442 [TBL] [Abstract][Full Text] [Related]
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