Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics
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Somatic/gonadal mosaicism for structural autosomal rearrangements: female predominance among carriers of gonadal mosaicism for unbalanced rearrangementsUnrevealed mosaicism in the next-generation sequencing eraMethods for comprehensive chromosome screening of oocytes and embryos: capabilities, limitations, and evidence of validityClinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concernsSomatic mosaicism: implications for disease and transmission geneticsHuman molecular cytogenetics: From cells to nucleotidesStructural variation mutagenesis of the human genome: Impact on disease and evolution.Mosaic structural variation in children with developmental disordersSomatic mosaicism underlies X-linked acrogigantism syndrome in sporadic male subjectsConsensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomaliesClinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases.Delineating the cytogenomic and epigenomic landscapes of glioma stem cell linesComparable low-level mosaicism in affected and non affected tissue of a complex CDH patientA fast and accurate method to detect allelic genomic imbalances underlying mosaic rearrangements using SNP array data.Identification of clinically important chromosomal aberrations in acute myeloid leukemia by array-based comparative genomic hybridization.Mosaic uniparental disomies and aneuploidies as large structural variants of the human genome.Chromosomal aberrations in bladder cancer: fresh versus formalin fixed paraffin embedded tissue and targeted FISH versus wide microarray-based CGH analysis.Piecing together the problems in diagnosing low-level chromosomal mosaicism.Chromosomal imbalances in human bladder urothelial carcinoma: similarities and differences between biopsy samples and cancer stem-like cellsComprehensive 5-year study of cytogenetic aberrations in 668 infertile menDNA copy number alterations and PPARG amplification in a patient with multifocal bladder urothelial carcinoma.Controlled somatic and germline copy number variation in the mouse modelComparative genomic hybridization on microarray (a-CGH) in constitutional and acquired mosaicism may detect as low as 8% abnormal cellsSomatic mosaicism detected by exon-targeted, high-resolution aCGH in 10,362 consecutive cases.Detection of clinically relevant exonic copy-number changes by array CGH.Molecular analysis of products of conception obtained by hysteroembryoscopy from infertile couples.Sensitive quantification of mosaicism using high density SNP arrays and the cumulative distribution function.Meiotic errors followed by two parallel postzygotic trisomy rescue events are a frequent cause of constitutional segmental mosaicism.Discordance between karyotype from amniotic fluid and postnatal lymphocyte culturesFrom cytogenomic to epigenomic profiles: monitoring the biologic behavior of in vitro cultured human bone marrow mesenchymal stem cells.Inducing segmental aneuploid mosaicism in the mouse through targeted asymmetric sister chromatid event of recombinationClinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 casesMicroarray-based mutation detection in the dystrophin gene.Microarray-based comparative genomic hybridization using sex-matched reference DNA provides greater sensitivity for detection of sex chromosome imbalances than array-comparative genomic hybridization with sex-mismatched reference DNAGenomic disorders ten years on.The biology of infertility: research advances and clinical challenges.Unexpected frequency of genomic alterations in histologically normal colonic tissue from colon cancer patients.Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis.Application of array comparative genomic hybridization in 256 patients with developmental delay or intellectual disability.Human embryonic stem cells and genomic instability.
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Microarray-based CGH detects chromosomal mosaicism not revealed by conventional cytogenetics
description
article
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im August 2007 veröffentlichter wissenschaftlicher Artikel
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wetenschappelijk artikel
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наукова стаття, опублікована у 2007
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name
Microarray-based CGH detects c ...... d by conventional cytogenetics
@en
Microarray-based CGH detects c ...... d by conventional cytogenetics
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type
label
Microarray-based CGH detects c ...... d by conventional cytogenetics
@en
Microarray-based CGH detects c ...... d by conventional cytogenetics
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Microarray-based CGH detects c ...... d by conventional cytogenetics
@en
Microarray-based CGH detects c ...... d by conventional cytogenetics
@nl
P2093
P356
P1476
Microarray-based CGH detects c ...... d by conventional cytogenetics
@en
P2093
A Craig Chinault
Amber Pursley
Andrea L Gropman
Ankita Patel
Anne M Summers
Arthur L Beaudet
Carlos A Bacino
Daryl A Scott
David T Miller
James R Lupski
P304
P356
10.1002/AJMG.A.31740
P407
P50
P577
2007-08-01T00:00:00Z