(Q37956500)

25 August 2017

title

From karyotyping to array-CGH in prenatal diagnosis (English)

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25 August 2017

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K D Lichtenbelt

1

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25 August 2017

N V A M Knoers

series ordinal

2

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25 August 2017

G H Schuring-Blom

series ordinal

3

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25 August 2017

publication date

12 November 2011

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Cytogenetics and Genome Research

25 August 2017

published in

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25 August 2017

volume

135

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25 August 2017

issue

3-4

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25 August 2017

page(s)

241-250

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Fetal sex determination using circulating cell-free fetal DNA (ccffDNA) at 11 to 13 weeks of gestation

25 August 2017

cites work

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Changes in the utilization of prenatal diagnosis

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Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?

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Revisiting the risk for aneuploidy in fetuses with isolated pyelectasis

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Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study

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Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray

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Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84.

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Prospective ranking of the sonographic markers for aneuploidy: data of 2143 prenatal cytogenetic diagnoses referred for abnormalities on ultrasound.

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What's new in karyotyping? The move towards array comparative genomic hybridisation (CGH).

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Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis

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Rapid methods for targeted prenatal diagnosis of common chromosome aneuploidies

21 January 2018

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aCGH on chorionic villi mirrors the complexity of fetoplacental mosaicism in prenatal diagnosis

21 January 2018

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Molecular hybridization of radioactive DNA to the DNA of cytological preparations

21 January 2018

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Non-invasive aneuploidy detection using free fetal DNA and RNA in maternal plasma: recent progress and future possibilities

21 January 2018

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Determination of fetal chromosome aberrations from fetal DNA in maternal blood: has the challenge finally been met?

21 January 2018

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Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis

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Bi-color detection of two target DNAs by non-radioactive in situ hybridization.

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Rapid and simple prenatal diagnosis of common chromosome disorders: advantages and disadvantages of the molecular methods FISH and QF-PCR.

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Incidence and significance of chromosome mosaicism involving an autosomal structural abnormality diagnosed prenatally through amniocentesis: a collaborative study

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Donnai-Barrow syndrome (DBS/FOAR) in a child with a homozygous LRP2 mutation due to complete chromosome 2 paternal isodisomy

21 January 2018

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Prenatal testing for uniparental disomy: indications and clinical relevance

21 January 2018

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Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations

21 January 2018

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Somatic mosaicism in cases with small supernumerary marker chromosomes

21 January 2018

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Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases

21 January 2018

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Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting.

21 January 2018

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Pregnancy complicated by triploidy: a comparison of the three karyotypes.

21 January 2018

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Array comparative genomic hybridization and flow cytometry analysis of spontaneous abortions and mors in utero samples.

21 January 2018

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Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

21 January 2018

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Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21.

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Application of a target array comparative genomic hybridization to prenatal diagnosis

21 January 2018

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Prenatal diagnosis by array-CGH.

21 January 2018

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Prenatal detection of unbalanced chromosomal rearrangements by array CGH.

21 January 2018

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Diagnosis of miscarriages by molecular karyotyping: benefits and pitfalls

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Comparative genomic hybridization-array analysis enhances the detection of aneuploidies and submicroscopic imbalances in spontaneous miscarriages

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21 January 2018

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21 January 2018

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21 January 2018

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21 January 2018

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Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation

21 January 2018

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High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings.

21 January 2018

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Comparative genomic hybridization and prenatal diagnosis

21 January 2018

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Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

21 January 2018

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How unexpected are unexpected findings in prenatal cytogenetic diagnosis? A literature review

21 January 2018

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Digital fetal aneuploidy diagnosis by next-generation sequencing

21 January 2018

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Fetal ultrasound abnormalities: correlation with fetal karyotype, autopsy findings, and postnatal outcome--five-year prospective study

21 January 2018

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Congenital heart disease and aneuploidy

21 January 2018

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Presence of fetal DNA in maternal plasma and serum

21 January 2018

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

21 January 2018

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21 January 2018

Identifiers

DOI

10.1159/000334065

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25 August 2017

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