Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization - Wikidata - awgldk - TriplyDB

Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization

Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization

http://www.wikidata.org/entity/Q57537925

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Clinical impact of copy number variation analysis using high-resolution microarray technologies: advantages, limitations and concerns Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011 Microarray comparative genomic hybridization in prenatal diagnosis: a review Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases.Whole genome scanning: resolving clinical diagnosis and management amidst complex data.Application of a target array comparative genomic hybridization to prenatal diagnosis.Non-invasive prenatal testing: ethical issues explored 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 'thousand-dollar genome': an ethical exploration.Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis.Targeted capture enrichment assay for non-invasive prenatal testing of large and small size sub-chromosomal deletions and duplications Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomalies Prenatal testing for intellectual disability: misperceptions and reality with lessons from Down syndrome.Controversies and challenges of array comparative genomic hybridization in prenatal genetic diagnosis.Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives.Bacterial artificial chromosome-emulation oligonucleotide arrays for targeted clinical array-comparative genomic hybridization analyses.The impact of human copy number variation on a new era of genetic testing.Copy-number changes in prenatal diagnosis.Clinical laboratory implementation of cytogenomic microarrays.From karyotyping to array-CGH in prenatal diagnosis.Genomic microarrays: a technology overview.Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.Detecting genomic imbalances in prenatal diagnosis: main hurdles and recent advances.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.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.Prenatal genetic diagnosis using microarray analysis in fetuses with congenital heart defects.Uncovering recurrent microdeletion syndromes and subtelomeric deletions/duplications through non-selective application of a MLPA-based extended prenatal panel in routine prenatal diagnosis.Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing.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.Prenatal detection of cryptic rearrangements by multiplex ligation probe amplification in fetuses with ultrasound abnormalities.The introduction of arrays in prenatal diagnosis: a special challenge.

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Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization

http://www.wikidata.org/entity/Q57537925

description

scientific article published on 01 November 2006

@en

wetenschappelijk artikel

@nl

наукова стаття, опублікована в листопаді 2006

@uk

name

Prenatal diagnosis of chromoso ...... parative genomic hybridization

@en

Prenatal diagnosis of chromoso ...... parative genomic hybridization

@nl

type

label

Prenatal diagnosis of chromoso ...... parative genomic hybridization

@en

Prenatal diagnosis of chromoso ...... parative genomic hybridization

@nl

prefLabel

Prenatal diagnosis of chromoso ...... parative genomic hybridization

@en

Prenatal diagnosis of chromoso ...... parative genomic hybridization

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01.GIM.0000245576.47154.63

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Genetics in Medicine

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Prenatal diagnosis of chromoso ...... parative genomic hybridization

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A Craig Chinault

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Ankita Patel

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Arthur L Beaudet

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Audrey Burke

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Benjamin B Roa

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Christine M Eng

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Daniela del Gaudio

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Ignatia B Van den Veyver

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Jiangzhen Li

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Patricia Ward

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P2860

Detection of large-scale variation in the human genome

Segmental duplications and copy-number variation in the human genome.

Large-scale copy number polymorphism in the human genome

High resolution analysis of DNA copy number variation using comparative genomic hybridization to microarrays

Comparative genomic hybridization for molecular cytogenetic analysis of solid tumors

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities.

Microarray analysis of cell-free fetal DNA in amniotic fluid: a prenatal molecular karyotype.

Prenatal diagnosis using interphase fluorescence in situ hybridization (FISH): 2-year multi-center retrospective study and review of the literature.

Circulating fetal DNA: its origin and diagnostic potential-a review.

Prenatal diagnosis by array-CGH.

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