204 related articles for article (PubMed ID: 21334567)
61. [Cerebral polymicrogyria and 22q11 deletion syndrome].
Arriola-Pereda G; Verdú-Pérez A; de Castro-De Castro P
Rev Neurol; 2009 Feb 16-28; 48(4):188-90. PubMed ID: 19226486
[TBL] [Abstract][Full Text] [Related]
62. Deviant dynamics of EEG resting state pattern in 22q11.2 deletion syndrome adolescents: A vulnerability marker of schizophrenia?
Tomescu MI; Rihs TA; Becker R; Britz J; Custo A; Grouiller F; Schneider M; Debbané M; Eliez S; Michel CM
Schizophr Res; 2014 Aug; 157(1-3):175-81. PubMed ID: 24962438
[TBL] [Abstract][Full Text] [Related]
63. Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study.
Campbell LE; Daly E; Toal F; Stevens A; Azuma R; Catani M; Ng V; van Amelsvoort T; Chitnis X; Cutter W; Murphy DG; Murphy KC
Brain; 2006 May; 129(Pt 5):1218-28. PubMed ID: 16569671
[TBL] [Abstract][Full Text] [Related]
64. Craniofacial dysmorphology in 22q11.2 deletion syndrome by 3D laser surface imaging and geometric morphometrics: illuminating the developmental relationship to risk for psychosis.
Prasad S; Katina S; Hennessy RJ; Murphy KC; Bowman AW; Waddington JL
Am J Med Genet A; 2015 Mar; 167A(3):529-36. PubMed ID: 25691406
[TBL] [Abstract][Full Text] [Related]
65. Association of the low-activity COMT 158Met allele with ADHD and OCD in subjects with velocardiofacial syndrome.
Gothelf D; Michaelovsky E; Frisch A; Zohar AH; Presburger G; Burg M; Aviram-Goldring A; Frydman M; Yeshaya J; Shohat M; Korostishevsky M; Apter A; Weizman A
Int J Neuropsychopharmacol; 2007 Jun; 10(3):301-8. PubMed ID: 16734939
[TBL] [Abstract][Full Text] [Related]
66. 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]
67. Dual-probe fluorescence in situ hybridization assay for detecting deletions associated with VCFS/DiGeorge syndrome I and DiGeorge syndrome II loci.
Berend SA; Spikes AS; Kashork CD; Wu JM; Daw SC; Scambler PJ; Shaffer LG
Am J Med Genet; 2000 Apr; 91(4):313-7. PubMed ID: 10766989
[TBL] [Abstract][Full Text] [Related]
68. DiGeorge/velocardiofacial syndrome: FISH studies of chromosomes 22q11 and 10p14, and clinical reports on the proximal 22q11 deletion.
Bartsch O; Nemecková M; Kocárek E; Wagner A; Puchmajerová A; Poppe M; Ounap K; Goetz P
Am J Med Genet A; 2003 Feb; 117A(1):1-5. PubMed ID: 12548732
[TBL] [Abstract][Full Text] [Related]
69. Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia.
Murphy KC; Owen MJ
Br J Psychiatry; 2001 Nov; 179():397-402. PubMed ID: 11689394
[TBL] [Abstract][Full Text] [Related]
70. The effects of gender and catechol O-methyltransferase (COMT) Val108/158Met polymorphism on emotion regulation in velo-cardio-facial syndrome (22q11.2 deletion syndrome): An fMRI study.
Coman IL; Gnirke MH; Middleton FA; Antshel KM; Fremont W; Higgins AM; Shprintzen RJ; Kates WR
Neuroimage; 2010 Nov; 53(3):1043-50. PubMed ID: 20123031
[TBL] [Abstract][Full Text] [Related]
71. Stranded, part II: Velocardiofacial syndrome, behavioral neurogenetics, and the study of developmental psychopathology.
Feinstein C
J Am Acad Child Adolesc Psychiatry; 2009 Nov; 48(11):1049-1050. PubMed ID: 19855217
[No Abstract] [Full Text] [Related]
72. [Microdeletion 22q11.2. A too rarely diagnosed genetic change in psychiatric illnesses].
Leyhe T; Haarmeier T; Dufke A; Giedke H
Nervenarzt; 2002 May; 73(5):452-7. PubMed ID: 12078024
[TBL] [Abstract][Full Text] [Related]
73. 22q11 DS: genomic mechanisms and gene function in DiGeorge/velocardiofacial syndrome.
Maynard TM; Haskell GT; Lieberman JA; LaMantia AS
Int J Dev Neurosci; 2002; 20(3-5):407-19. PubMed ID: 12175881
[TBL] [Abstract][Full Text] [Related]
74. DiGeorge syndrome/velocardiofacial syndrome: the chromosome 22q11.2 deletion syndrome.
Sullivan KE
Adv Exp Med Biol; 2007; 601():37-49. PubMed ID: 17712990
[TBL] [Abstract][Full Text] [Related]
75. A comparative study of hearing loss in two microdeletion syndromes: velocardiofacial (22q11.2 deletion) and Williams (7q11.23 deletion) syndromes.
Zarchi O; Attias J; Raveh E; Basel-Vanagaite L; Saporta L; Gothelf D
J Pediatr; 2011 Feb; 158(2):301-6. PubMed ID: 20846670
[TBL] [Abstract][Full Text] [Related]
76. Chromosome 22q11.2 deletion syndrome: DiGeorge syndrome/velocardiofacial Syndrome.
Sullivan KE
Immunol Allergy Clin North Am; 2008 May; 28(2):353-66. PubMed ID: 18424337
[TBL] [Abstract][Full Text] [Related]
77. Developmental changes in multivariate neuroanatomical patterns that predict risk for psychosis in 22q11.2 deletion syndrome.
Gothelf D; Hoeft F; Ueno T; Sugiura L; Lee AD; Thompson P; Reiss AL
J Psychiatr Res; 2011 Mar; 45(3):322-31. PubMed ID: 20817203
[TBL] [Abstract][Full Text] [Related]
78. Altered auditory processing in frontal and left temporal cortex in 22q11.2 deletion syndrome: a group at high genetic risk for schizophrenia.
Rihs TA; Tomescu MI; Britz J; Rochas V; Custo A; Schneider M; Debbané M; Eliez S; Michel CM
Psychiatry Res; 2013 May; 212(2):141-9. PubMed ID: 23137800
[TBL] [Abstract][Full Text] [Related]
79. 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]
80. Independent de novo 22q11.2 deletions in first cousins with DiGeorge/velocardiofacial syndrome.
Saitta SC; Harris SE; McDonald-McGinn DM; Emanuel BS; Tonnesen MK; Zackai EH; Seitz SC; Driscoll DA
Am J Med Genet A; 2004 Jan; 124A(3):313-7. PubMed ID: 14708107
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]