Related references
Note: Only part of the references are listed.Differential gene expression in the hippocampus of the Df1/+ mice:: A model for 22q11.2 deletion syndrome and schizophrenia
Sinthuja Sivagnanasundaram et al.
BRAIN RESEARCH (2007)
Human TBX1 missense mutations cause gain of function resulting in the same phenotype as 22q11.2 deletions
Christiane Zweier et al.
AMERICAN JOURNAL OF HUMAN GENETICS (2007)
Corpus callosum morphology and ventricular size in chromosome 22q11.2 deletion syndrome
Alexei M. C. Machado et al.
BRAIN RESEARCH (2007)
Molecular characterization of deletion breakpoints in adults with 22q11 deletion syndrome
Rosanna Weksberg et al.
HUMAN GENETICS (2007)
Gene dosage in the developing and adult brain in a mouse model of 22q11 deletion syndrome
D. W. Meechan et al.
MOLECULAR AND CELLULAR NEUROSCIENCE (2006)
Polymicrogyria and deletion 22q11.2 syndrome: Window to the etiology of a common cortical malformation
Nathaniel H. Robin et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
Behavior of mice with mutations in the conserved region deleted in velocardiofacial/DiGeorge syndrome
Jeffrey M. Long et al.
NEUROGENETICS (2006)
Dissection of Tbx1 and Fgf interactions in mouse models of 22q11DS suggests functional redundancy
Vimla S. Aggarwal et al.
HUMAN MOLECULAR GENETICS (2006)
Neurocognitive profile in 22q11 deletion syndrome and schizophrenia
Eva W. C. Chow et al.
SCHIZOPHRENIA RESEARCH (2006)
Genetic malformations of cortical development
Renzo Guerrini et al.
EXPERIMENTAL BRAIN RESEARCH (2006)
Periventricular nodular heterotopia and Williams syndrome
Russell J. Ferland et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2006)
Specific cerebellar reductions in children with chromosome 22q11.2 deletion syndrome
Joel P. Bish et al.
NEUROSCIENCE LETTERS (2006)
Tbx1 haploinsufficiency is linked to behavioral disorders in mice and humans:: Implications for 22q11 deletion syndrome
Richard Paylor et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2006)
Brain and behaviour in children with 22q11.2 deletion syndrome: a volumetric and voxel-based morphometry MRI study
LE Campbell et al.
BRAIN (2006)
Crkl deficiency disrupts Fgf8 signaling in a mouse model of 22q11 deletion syndromes
AM Moon et al.
DEVELOPMENTAL CELL (2006)
Dose-dependent interaction of Tbx1 and Crkl and locally aberrant RA signaling in a model of del22q11 syndrome
DL Guris et al.
DEVELOPMENTAL CELL (2006)
Clinical features of 78 adults with 22q11 deletion syndrome
AS Bassett et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2005)
Volumetric, connective, and morphologic changes in the brains of children with chromosome 22q11.2 deletion syndrome: an integrative study
TJ Simon et al.
NEUROIMAGE (2005)
A survey of the 22q11 microdeletion in a large cohort of schizophrenia patients
A Horowitz et al.
SCHIZOPHRENIA RESEARCH (2005)
The expression of retinoic acid receptor alpha is increased in the granule cells of the dentate gyrus in schizophrenia
L Rioux et al.
PSYCHIATRY RESEARCH (2005)
Frontal and caudate alterations in velocardiofacial syndrome (Deletion at chromosome 22q11.2)
WR Kates et al.
JOURNAL OF CHILD NEUROLOGY (2004)
Abnormalities of the corpus callosum in nonpsychotic children with chromosome 22q11 deletion syndrome
V Shashi et al.
NEUROIMAGE (2004)
Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion
SC Saitta et al.
HUMAN MOLECULAR GENETICS (2004)
Incidence and prevalence of the 22q11 deletion syndrome:: a population-based study in Western Sweden
S Oskarsdóttir et al.
ARCHIVES OF DISEASE IN CHILDHOOD (2004)
Chromosome 22q11 deletion and pachygyria characterized by array-based comparative genomic hybridization
DA Koolen et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2004)
Drug-induced stimulation and suppression of action monitoring in healthy volunteers
ERA de Bruijn et al.
PSYCHOPHARMACOLOGY (2004)
Brain anatomy in adults with velocardiofacial syndrome with and without schizophrenia - Preliminary results of a structural magnetic resonance Imaging study
T van Amelsvoort et al.
ARCHIVES OF GENERAL PSYCHIATRY (2004)
A comprehensive analysis of 22q11 gene expression in the developing and adult brain
TM Maynard et al.
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA (2003)
The schizophrenia phenotype in 22q11 deletion syndrome
AS Bassett et al.
AMERICAN JOURNAL OF PSYCHIATRY (2003)
VEGF:: A modifier of the del22q11 (DiGeorge) syndrome?
I Stalmans et al.
NATURE MEDICINE (2003)
Size of hippocampal pyramidal neurons in schizophrenia
JR Highley et al.
BRITISH JOURNAL OF PSYCHIATRY (2003)
Structural brain abnormalities in patients with schizophrenia and 22q11 Deletion Syndrome
EWC Chow et al.
BIOLOGICAL PSYCHIATRY (2002)
Patterns of dysmorphic features in schizophrenia
LE Scutt et al.
AMERICAN JOURNAL OF MEDICAL GENETICS (2001)
Mice lacking the homologue of the human 22q11.2 gene CRKL phenocopy neurocristopathies of DiGeorge syndrome
DL Guris et al.
NATURE GENETICS (2001)
Cortical dysgenesis in 2 patients with chromosome 22q11 deletion
LM Bird et al.
CLINICAL GENETICS (2000)
Share Paper
