about
Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders.New insights into the regulatory function of CYFIP1 in the context of WAVE- and FMRP-containing complexes.Monogenic and chromosomal causes of isolated speech and language impairment.Chromosomal Microarray Analysis of Consecutive Individuals with Autism Spectrum Disorders Using an Ultra-High Resolution Chromosomal Microarray Optimized for Neurodevelopmental Disorders.High-resolution chromosome ideogram representation of currently recognized genes for autism spectrum disordersPrader-Willi syndrome: a review of clinical, genetic, and endocrine findings.MLPA analysis in a cohort of patients with autism.Copy number variation profile in the placental and parental genomes of recurrent pregnancy loss families.GeneAnalytics Pathway Analysis and Genetic Overlap among Autism Spectrum Disorder, Bipolar Disorder and Schizophrenia.New discoveries in schizophrenia genetics reveal neurobiological pathways: A review of recent findings.Modeling psychiatric disorders with patient-derived iPSCs.Autism: a transdiagnostic, dimensional, construct of reasoning?An update on the comorbidity of ADHD and ASD: a focus on clinical management.Copy Number Variations in Amyotrophic Lateral Sclerosis: Piecing the Mosaic Tiles Together through a Systems Biology Approach.Modeling neurodevelopmental and psychiatric diseases with human iPSCs.Recurrent 15q11.2 BP1-BP2 microdeletions and microduplications in the etiology of neurodevelopmental disorders."Something Extra on Chromosome 5": Parents' Understanding of Positive Prenatal Chromosomal Microarray Analysis (CMA) Results.Genetic and morphological features of human iPSC-derived neurons with chromosome 15q11.2 (BP1-BP2) deletionsVariable Penetrance of the 15q11.2 BP1-BP2 Microduplication in a Family with Cognitive and Language Impairment.Clinical and genetic aspects of the 15q11.2 BP1-BP2 microdeletion disorder.Prader-Willi syndrome genetic subtypes and clinical neuropsychiatric diagnoses in residential care adults.SNP array screening of cryptic genomic imbalances in 450 Japanese subjects with intellectual disability and multiple congenital anomalies previously negative for large rearrangements.Syndromic autism spectrum disorders: moving from a clinically defined to a molecularly defined approach.Low-Density Neuronal Cultures from Human Induced Pluripotent Stem Cells.Major Contribution of Genomic Copy Number Variation in Syndromic Congenital Heart Disease: The Use of MLPA as the First Genetic Test.Analysis copy number variation of Chinese children in early-onset epileptic encephalopathies with unknown cause.Robust identification of deletions in exome and genome sequence data based on clustering of Mendelian errors.Second-trimester fetal autopsy: A morphological study with prenatal USG correlations and clinical implications
P2860
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P2860
description
2015 nî lūn-bûn
@nan
2015 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2015 թվականի փետրվարին հրատարակված գիտական հոդված
@hy
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
name
The 15q11.2 BP1-BP2 microdeletion syndrome: a review
@ast
The 15q11.2 BP1-BP2 microdeletion syndrome: a review
@en
The 15q11.2 BP1-BP2 microdeletion syndrome: a review
@nl
type
label
The 15q11.2 BP1-BP2 microdeletion syndrome: a review
@ast
The 15q11.2 BP1-BP2 microdeletion syndrome: a review
@en
The 15q11.2 BP1-BP2 microdeletion syndrome: a review
@nl
prefLabel
The 15q11.2 BP1-BP2 microdeletion syndrome: a review
@ast
The 15q11.2 BP1-BP2 microdeletion syndrome: a review
@en
The 15q11.2 BP1-BP2 microdeletion syndrome: a review
@nl
P2860
P356
P1476
The 15q11.2 BP1-BP2 microdeletion syndrome: a review
@en
P2093
Merlin G Butler
P2860
P304
P356
10.3390/IJMS16024068
P407
P50
P5008
P577
2015-02-13T00:00:00Z