about
Genetics of bipolar disorderBehavioural phenotypes and special educational needs: is aetiology important in the classroom?In search of the optimal surgical treatment for velopharyngeal dysfunction in 22q11.2 deletion syndrome: a systematic reviewEpigenetic mechanisms in cardiac development and diseaseConnecting teratogen-induced congenital heart defects to neural crest cells and their effect on cardiac functionThe neural crest in cardiac congenital anomaliesChimeric negative regulation of p14ARF and TBX1 by a t(9;22) translocation associated with melanoma, deafness, and DNA repair deficiencyChromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.Variability in Clinical and Anatomical Manifestation of Velocardiofacial Syndrome Presents Diagnostic and Policy Uncertainty.Persistent gating deficit and increased sensitivity to NMDA receptor antagonism after puberty in a new mouse model of the human 22q11.2 microdeletion syndrome: a study in male mice.Bridging the gene-behavior divide through neuroimaging deletion syndromes: Velocardiofacial (22q11.2 Deletion) and Williams (7q11.23 Deletion) syndromes.Feasibility and preliminary efficacy data from a computerized cognitive intervention in children with chromosome 22q11.2 deletion syndrome.Heterogeneity within Autism Spectrum Disorders: What have We Learned from Neuroimaging Studies?The PHF21B gene is associated with major depression and modulates the stress response.Autism genetics: emerging data from genome-wide copy-number and single nucleotide polymorphism scans.Velo-Cardio-Facial Syndrome.No evidence for the presence of genetic variants predisposing to psychotic disorders on the non-deleted 22q11.2 allele of VCFS patients.Applicability of the nonverbal learning disability paradigm for children with 22q11.2 deletion syndrome.The development of cognitive control in children with chromosome 22q11.2 deletion syndromeAssociation of the family environment with behavioural and cognitive outcomes in children with chromosome 22q11.2 deletion syndrome.Mediator and human diseaseTbx1 is required autonomously for cell survival and fate in the pharyngeal core mesoderm to form the muscles of mastication.Histology of the pharyngeal constrictor muscle in 22q11.2 deletion syndrome and non-syndromic children with velopharyngeal insufficiencyPlatybasia in 22q11.2 deletion syndrome is not correlated with speech resonance.Increased incidence and size of cavum septum pellucidum in children with chromosome 22q11.2 deletion syndrome.Shape-based classification of 3D facial data to support 22q11.2DS craniofacial research.Genome-wide approaches to schizophrenia.Socioeconomic status and psychological function in children with chromosome 22q11.2 deletion syndrome: implications for genetic counselingDiGeorge Syndrome: a not so rare disease.Multiplexed quantitative real-time PCR to detect 22q11.2 deletion in patients with congenital heart disease.Self-reported speech problems in adolescents and young adults with 22q11.2 deletion syndrome: a cross-sectional cohort study.Characteristic face: a key indicator for direct diagnosis of 22q11.2 deletions in Chinese velocardiofacial syndrome patients.How might stress contribute to increased risk for schizophrenia in children with chromosome 22q11.2 deletion syndrome?A tale worth telling: the impact of the diagnosis experience on disclosure of genetic disorders.Keratoconus in an adult with 22q11.2 deletion syndromePremature death in adults with 22q11.2 deletion syndrome.An interictal schizophrenia-like psychosis in an adult patient with 22q11.2 deletion syndrome.Disrupted fornix integrity in children with chromosome 22q11.2 deletion syndromeIncidental radiologic findings in the 22q11.2 deletion syndromeAberrant Cortical Morphometry in the 22q11.2 Deletion Syndrome.
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2008 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
name
Velo-cardio-facial syndrome: 30 Years of study.
@ast
Velo-cardio-facial syndrome: 30 Years of study.
@en
Velo-cardio-facial syndrome: 30 Years of study.
@nl
type
label
Velo-cardio-facial syndrome: 30 Years of study.
@ast
Velo-cardio-facial syndrome: 30 Years of study.
@en
Velo-cardio-facial syndrome: 30 Years of study.
@nl
prefLabel
Velo-cardio-facial syndrome: 30 Years of study.
@ast
Velo-cardio-facial syndrome: 30 Years of study.
@en
Velo-cardio-facial syndrome: 30 Years of study.
@nl
P2860
P356
P1476
Velo-cardio-facial syndrome: 30 Years of study.
@en
P2093
Robert J Shprintzen
P2860
P356
10.1002/DDRR.2
P577
2008-01-01T00:00:00Z