Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.
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Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasoundGenomic microarray in fetuses with increased nuchal translucency and normal karyotype: a systematic review and meta-analysisMicroarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011Microarray comparative genomic hybridization in prenatal diagnosis: a reviewSNP arrays: comparing diagnostic yields for four platforms in children with developmental delay.From prenatal genomic diagnosis to fetal personalized medicine: progress and challenges.Prenatal diagnosis of a de novo interstitial deletion of 11q (11q22.3 → q23.3) associated with abnormal ultrasound findings by array comparative genomic hybridization.Large cryptic genomic rearrangements with apparently normal karyotypes detected by array-CGHAn improved method to extract DNA from 1 ml of uncultured amniotic fluid from patients at less than 16 weeks' gestation.The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a review of the literature.Prenatal Diagnosis of Central Nervous System Anomalies by High-Resolution Chromosomal Microarray Analysis.Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomaliesExperience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies.Dandy-Walker malformation and Wisconsin syndrome: novel cases add further insight into the genotype-phenotype correlations of 3q23q25 deletions.Array-based comparative genomic hybridization in 190 Korean patients with developmental delay and/or intellectual disability: a single tertiary care university center studyA prenatal missed diagnosed case of submicroscopic chromosomal abnormalities by karyotyping: the clinical utility of array-based CGH in prenatal diagnostics.Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis.Microarray-based prenatal diagnosis for the identification of fetal chromosome abnormalities.Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature.Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities.Prenatal Diagnosis of Cystic Hygroma related to a Deletion of 16q24.1 with Haploinsufficiency of FOXF1 and FOXC2 Genes.Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis.Prenatal diagnosis: array comparative genomic hybridization in fetuses with abnormal sonographic findings.Implementation of high-resolution SNP arrays in the investigation of fetuses with ultrasound malformations: 5 years of clinical experience.Application of chromosomal microarray analysis in prenatal diagnosis of fetal growth restriction.Prenatal diagnosis of trisomy 21, 18 and 13 by quantitative pyrosequencing of segmental duplications.De Novo 3q22.3q24 Microdeletion in a Patient With Blepharophimosis-Ptosis-Epicanthus Inversus Syndrome, Dandy-Walker Malformation, and Wisconsin Syndrome.The introduction of arrays in prenatal diagnosis: a special challenge.High-resolution microarray in the assessment of fetal anomalies detected by ultrasound
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P2860
Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.
description
2011 nî lūn-bûn
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2011年の論文
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2011年学术文章
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2011年学术文章
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2011年学术文章
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name
Whole-genome array CGH identif ...... ations and a normal karyotype.
@en
Whole-genome array CGH identif ...... ations and a normal karyotype.
@nl
type
label
Whole-genome array CGH identif ...... ations and a normal karyotype.
@en
Whole-genome array CGH identif ...... ations and a normal karyotype.
@nl
prefLabel
Whole-genome array CGH identif ...... ations and a normal karyotype.
@en
Whole-genome array CGH identif ...... ations and a normal karyotype.
@nl
P2093
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Whole-genome array CGH identif ...... mations and a normal karyotype
@en
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J L Michaud
V Désilets
P2860
P304
P356
10.1111/J.1399-0004.2011.01687.X
P577
2011-05-16T00:00:00Z