Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype
about
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-analysisClinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concernsMicroarray 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 reviewThe future of prenatal cytogenetic diagnostics: a personal perspective.From prenatal genomic diagnosis to fetal personalized medicine: progress and challenges.Molecular cytogenetic diagnosis and somatic genome variations.Meeting the challenge of interpreting high-resolution single nucleotide polymorphism array data in prenatal diagnosis: does increased diagnostic power outweigh the dilemma of rare variants?Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trial.An 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.Evolving applications of microarray analysis in prenatal diagnosis.Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flowArray 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.Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalitiesA prenatal missed diagnosed case of submicroscopic chromosomal abnormalities by karyotyping: the clinical utility of array-based CGH in prenatal diagnostics.Copy-number changes in prenatal diagnosis.Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.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.Prenatal and postnatal findings in a 10.6 Mb interstitial deletion at 10p11.22-p12.31.aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosis.Implementation of high resolution whole genome array CGH in the prenatal clinical setting: advantages, challenges, and review of the literature.Referral patterns for microarray testing in prenatal diagnosis.Prenatal microarray analysis as second-tier diagnostic test: single-center prospective study.Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis.Application of chromosomal microarray in the evaluation of abnormal prenatal findings.Implementation of high-resolution SNP arrays in the investigation of fetuses with ultrasound malformations: 5 years of clinical experience.Prenatal diagnosis using combined quantitative fluorescent polymerase chain reaction and array comparative genomic hybridization analysis as a first-line test: results from over 1000 consecutive cases.Impact of nationwide health insurance coverage for non-invasive prenatal testing.408 kb 15q11.2 microduplication by array comparative genomic hybridization in a fetus presenting with exomphalos, micrognathia, tetralogy of Fallot and normal karyotype: a genetic counseling dilemma in paternal carrier status.Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing.Prenatal diagnosis by chromosomal microarray analysis.The development of a rapid assay for prenatal testing of common aneuploidies and microdeletion syndromes.Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.The introduction of arrays in prenatal diagnosis: a special challenge.An economic analysis of prenatal cytogenetic technologies for sonographically detected fetal anomalies.
P2860
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P2860
Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype
description
2009 nî lūn-bûn
@nan
2009年の論文
@ja
2009年論文
@yue
2009年論文
@zh-hant
2009年論文
@zh-hk
2009年論文
@zh-mo
2009年論文
@zh-tw
2009年论文
@wuu
2009年论文
@zh
2009年论文
@zh-cn
name
Use of array comparative genom ...... and normal metaphase karyotype
@ast
Use of array comparative genom ...... and normal metaphase karyotype
@en
type
label
Use of array comparative genom ...... and normal metaphase karyotype
@ast
Use of array comparative genom ...... and normal metaphase karyotype
@en
prefLabel
Use of array comparative genom ...... and normal metaphase karyotype
@ast
Use of array comparative genom ...... and normal metaphase karyotype
@en
P2093
P2860
P356
P1433
P1476
Use of array comparative genom ...... and normal metaphase karyotype
@en
P2093
Diana W Bianchi
Emily Rorem
Hocine Tighiouart
Janet Cowan
Linda Kleeman
Lisa G Shaffer
Louise E Wilkins-Haug
Sabrina D Craigo
P2860
P304
P356
10.1002/PD.2367
P577
2009-12-01T00:00:00Z