Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.
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Genetic Counseling for Autism Spectrum Disorder in an Evolving Theoretical LandscapeA Subset of Autism-Associated Genes Regulate the Structural Stability of Neurons.Terminal chromosome 4q deletion syndrome in an infant with hearing impairment and moderate syndromic features: review of literature.Clinical Presentation and Microarray Analysis of Peruvian Children with Atypical Development and/or Aberrant BehaviorChromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.Whole exome sequencing in females with autism implicates novel and candidate genes.High-resolution chromosome ideogram representation of currently recognized genes for autism spectrum disordersLanguage impairment and dyslexia genes influence language skills in children with autism spectrum disorders.Routine chromosomal microarray analysis is necessary in Korean patients with unexplained developmental delay/mental retardation/autism spectrum disorder.Increased burden of de novo predicted deleterious variants in complex congenital diaphragmatic hernia.A recurrent deletion on chromosome 2q13 is associated with developmental delay and mild facial dysmorphisms.New insights in the interpretation of array-CGH: autism spectrum disorder and positive family history for intellectual disability predict the detection of pathogenic variants.Parents' perceptions of the usefulness of chromosomal microarray analysis for children with autism spectrum disordersCytogenetic and Clinical Features in Children Suspected With Congenital Abnormalities in 1 Medical Center of Zhejiang Province From 2011 to 2014An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity DisorderDiagnostic yield of array CGH in patients with autism spectrum disorder in Hong KongClinical Performance of an Ultrahigh Resolution Chromosomal Microarray Optimized for Neurodevelopmental DisordersParkin Deficiency Reduces Hippocampal Glutamatergic Neurotransmission by Impairing AMPA Receptor Endocytosis.The complex genetics in autism spectrum disorders.Genetic architecture, epigenetic influence and environment exposure in the pathogenesis of Autism.SNARE complex in developmental psychiatry: neurotransmitter exocytosis and beyond.Chromosomal Microarrays: Understanding Genetics of Neurodevelopmental Disorders and Congenital Anomalies.Duplication of the NPHP1 gene in patients with autism spectrum disorder and normal intellectual ability: a case series.Chromosomal microarray analysis in a cohort of underrepresented population identifies SERINC2 as a novel candidate gene for autism spectrum disorder.Behavioral and neuroanatomical analyses in a genetic mouse model of 2q13 duplication.Conditional neuroligin-2 knockout in adult medial prefrontal cortex links chronic changes in synaptic inhibition to cognitive impairments.Clinical and genetic aspects of the 15q11.2 BP1-BP2 microdeletion disorder.Clinical application of SNP array analysis in fetuses with ventricular septal defects and normal karyotypes.An atypical autistic phenotype associated with a 2q13 microdeletion: a case report.Copy number variants implicate cardiac function and development pathways in earthquake-induced stress cardiomyopathy.Delineating the psychiatric and behavioral phenotype of recurrent 2q13 deletions and duplications.Parkinson's disease-linked Parkin mutations impair glutamatergic signaling in hippocampal neurons
P2860
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P2860
Chromosomal microarray analysis of consecutive individuals with autism spectrum disorders or learning disability presenting for genetic services.
description
2013 nî lūn-bûn
@nan
2013 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2013 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2013年の論文
@ja
2013年論文
@yue
2013年論文
@zh-hant
2013年論文
@zh-hk
2013年論文
@zh-mo
2013年論文
@zh-tw
2013年论文
@wuu
name
Chromosomal microarray analysi ...... esenting for genetic services.
@ast
Chromosomal microarray analysi ...... esenting for genetic services.
@en
type
label
Chromosomal microarray analysi ...... esenting for genetic services.
@ast
Chromosomal microarray analysi ...... esenting for genetic services.
@en
prefLabel
Chromosomal microarray analysi ...... esenting for genetic services.
@ast
Chromosomal microarray analysi ...... esenting for genetic services.
@en
P2093
P2860
P921
P3181
P1433
P1476
Chromosomal microarray analysi ...... esenting for genetic services.
@en
P2093
Jennifer L Roberts
Karine Hovanes
Majed Dasouki
Merlin G Butler
P2860
P3181
P356
10.1016/J.GENE.2013.10.020
P407
P577
2013-11-02T00:00:00Z