(Q38125160)

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Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature

scientific article published on February 2014

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

29 August 2017

Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature (English)

1 reference

Europe PubMed Central

PubMed publication ID

29 August 2017

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systematic review

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based on heuristic

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author name string

M C de Wit

1

1 reference

Europe PubMed Central

PubMed publication ID

29 August 2017

M I Srebniak

2

1 reference

Europe PubMed Central

PubMed publication ID

29 August 2017

L C P Govaerts

3

1 reference

Europe PubMed Central

PubMed publication ID

29 August 2017

D Van Opstal

4

1 reference

Europe PubMed Central

PubMed publication ID

29 August 2017

R J H Galjaard

5

1 reference

Europe PubMed Central

PubMed publication ID

29 August 2017

A T J I Go

6

1 reference

Europe PubMed Central

PubMed publication ID

29 August 2017

publication date

1 February 2014

1 reference

Europe PubMed Central

PubMed publication ID

29 August 2017

Ultrasound in Obstetrics and Gynecology

1 reference

Europe PubMed Central

PubMed publication ID

29 August 2017

43

1 reference

Europe PubMed Central

PubMed publication ID

29 August 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

29 August 2017

139-146

1 reference

Europe PubMed Central

PubMed publication ID

29 August 2017

Ultrasonographically detectable markers of fetal chromosomal abnormalities

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Detection of large-scale variation in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Global variation in copy number in the human genome

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

A copy number variation morbidity map of developmental delay

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

First-trimester septated cystic hygroma: prevalence, natural history, and pediatric outcome

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Prenatal genetic diagnosis using microarray analysis in fetuses with congenital heart defects

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Prenatal microarray analysis as second-tier diagnostic test: single-center prospective study

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Prenatal diagnosis: array comparative genomic hybridization in fetuses with abnormal sonographic findings

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Detection rates of clinically significant genomic alterations by microarray analysis for specific anomalies detected by ultrasound

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Prenatal diagnosis of chromosomal abnormalities in fetuses with abnormal cardiac ultrasound findings: evaluation of chromosomal microarray-based analysis

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

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?

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

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.

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Challenges of interpreting copy number variation in syndromic and non-syndromic congenital heart defects.

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

High frequency of submicroscopic genomic aberrations detected by tiling path array comparative genome hybridisation in patients with isolated congenital heart disease.

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Implementation of high resolution whole genome array CGH in the prenatal clinical setting: advantages, challenges, and review of the literature

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomalies

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Chromosomal microarray versus karyotyping for prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Application of chromosomal microarray in the evaluation of abnormal prenatal findings

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities.

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Prenatal diagnosis using array-CGH: a French experience.

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Cryptic Chromosomal Abnormalities Identified in Children With Congenital Heart Disease

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12575

21 January 2018

Identifiers

10.1002/UOG.12575

1 reference

Europe PubMed Central

PubMed publication ID

29 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

29 August 2017

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