Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance.
about
Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomaliesGenome-wide oligonucleotide array comparative genomic hybridization for etiological diagnosis of mental retardation: a multicenter experience of 1499 clinical cases.Microdeletion/duplication at 15q13.2q13.3 among individuals with features of autism and other neuropsychiatric disorders.Genetic tools and algorithms for gene discovery in major congenital anomalies.Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance.MLPA for confirmation of array CGH results and determination of inheritance.Microdeletion and microduplication analysis of chinese conotruncal defects patients with targeted array comparative genomic hybridizationTBX6 null variants and a common hypomorphic allele in congenital scoliosis.Translocation t(11;14) (q13;q32) and genomic imbalances in multi-ethnic multiple myeloma patients: a Malaysian study.Array-based comparative genomic hybridization in 190 Korean patients with developmental delay and/or intellectual disability: a single tertiary care university center studyDownregulated microRNA-200a in meningiomas promotes tumor growth by reducing E-cadherin and activating the Wnt/beta-catenin signaling pathway.Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects.A recurrent 1.71 Mb genomic imbalance at 2q13 increases the risk of developmental delay and dysmorphism.Genome arrays for the detection of copy number variations in idiopathic mental retardation, idiopathic generalized epilepsy and neuropsychiatric disorders: lessons for diagnostic workflow and research.Nucleic acid-based diagnostics for infectious diseases in public health affairs.Prenatal diagnosis by array-comparative genomic hybridization.SOX12 and NRSN2 are candidate genes for 20p13 subtelomeric deletions associated with developmental delay.Custom Array Comparative Genomic Hybridization: the Importance of DNA Quality, an Expert Eye, and Variant Validation.Oligonucleotide microarrays for clinical diagnosis of copy number variation and zygosity status.Intra-family phenotypic heterogeneity of 16p11.2 deletion carriers in a three-generation Chinese family.Clinical application of array-based comparative genomic hybridization by two-stage screening for 536 patients with mental retardation and multiple congenital anomalies.DNA sensor by using electrochemiluminescence of acridinium ester initiated by tripropylamine.Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization.Application of dual-genome oligonucleotide array-based comparative genomic hybridization to the molecular diagnosis of mitochondrial DNA deletion and depletion syndromes.
P2860
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P2860
Development of a focused oligonucleotide-array comparative genomic hybridization chip for clinical diagnosis of genomic imbalance.
description
2007 nî lūn-bûn
@nan
2007 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Development of a focused oligo ...... iagnosis of genomic imbalance.
@ast
Development of a focused oligo ...... iagnosis of genomic imbalance.
@en
Development of a focused oligo ...... iagnosis of genomic imbalance.
@nl
type
label
Development of a focused oligo ...... iagnosis of genomic imbalance.
@ast
Development of a focused oligo ...... iagnosis of genomic imbalance.
@en
Development of a focused oligo ...... iagnosis of genomic imbalance.
@nl
prefLabel
Development of a focused oligo ...... iagnosis of genomic imbalance.
@ast
Development of a focused oligo ...... iagnosis of genomic imbalance.
@en
Development of a focused oligo ...... iagnosis of genomic imbalance.
@nl
P2093
P1433
P1476
Development of a focused oligo ...... iagnosis of genomic imbalance.
@en
P2093
Bai-Lin Wu
Christopher A Walsh
David T Miller
Hung Siv Tang
Keith Tomaszewicz
Mira Irons
Orah Platt
Sau Wai Cheung
P304
P356
10.1373/CLINCHEM.2007.090290
P407
P577
2007-09-27T00:00:00Z