These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
3. 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]
4. 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]
5. The velocardiofacial syndrome in older age: dementia and autistic features. Evers LJ; Vermaak MP; Engelen JJ; Curfs LM Genet Couns; 2006; 17(3):333-40. PubMed ID: 17100202 [TBL] [Abstract][Full Text] [Related]
6. Cognitive phenotype of velocardiofacial syndrome: a review. Furniss F; Biswas AB; Gumber R; Singh N Res Dev Disabil; 2011; 32(6):2206-13. PubMed ID: 21764255 [TBL] [Abstract][Full Text] [Related]
13. 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]
14. Prospective control abilities during visuo-manual tracking in children with 22q11.2 Deletion syndrome compared to age- and IQ-matched controls. Van Aken K; Swillen A; Beirinckx M; Janssens L; Caeyenberghs K; Smits-Engelsman B Res Dev Disabil; 2010; 31(3):634-41. PubMed ID: 20181458 [TBL] [Abstract][Full Text] [Related]
15. 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]
20. 22q13.3 deletion syndrome: a recognizable malformation syndrome associated with marked speech and language delay. Cusmano-Ozog K; Manning MA; Hoyme HE Am J Med Genet C Semin Med Genet; 2007 Nov; 145C(4):393-8. PubMed ID: 17926345 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]