(Q37735343)

English

A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings

scientific article published on 22 April 2014

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings (English)

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

0 references

author name string

Joo Wook Ahn

1

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

Susan Bint

2

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

Melita D Irving

3

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

Phillipa M Kyle

4

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

Ranjit Akolekar

5

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

Shehla N Mohammed

6

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

Caroline Mackie Ogilvie

7

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

publication date

22 April 2014

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

2

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

e354

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

An exploration of genetic counselors' needs and experiences with prenatal chromosomal microarray testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

22 August 2017

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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

22 August 2017

Chromosomal microarray versus karyotyping for prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

22 August 2017

Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

22 August 2017

Women's experiences receiving abnormal prenatal chromosomal microarray testing results

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

22 August 2017

DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

22 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

22 August 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

22 August 2017

Application of a target array comparative genomic hybridization to prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

22 August 2017

QF-PCR as a stand-alone test for prenatal samples: the first 2 years' experience in the London region

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

22 August 2017

Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

22 August 2017

Ethical controversies in prenatal microarray

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

6 September 2017

Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals - results from four years' clinical application for over 8,700 patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

14 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

23 June 2018

Correlation between Waardenburg syndrome phenotype and genotype in a population of individuals with identified PAX3 mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

23 June 2018

A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

1 September 2018

Implementation of high-resolution SNP arrays in the investigation of fetuses with ultrasound malformations: 5 years of clinical experience

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

1 September 2018

Prenatal chromosomal microarray analysis: a survey of prenatal genetic counselors' experiences and attitudes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

1 September 2018

The introduction of arrays in prenatal diagnosis: a special challenge.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

1 September 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://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4006225

1 September 2018

Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/24795849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens

1 reference

https://pubmed.ncbi.nlm.nih.gov/24795849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

De novobalanced chromosome rearrangements in prenatal diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/24795849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Controversies in prenatal diagnosis 3: should everyone undergoing invasive testing have a microarray?

1 reference

https://pubmed.ncbi.nlm.nih.gov/24795849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

How does altering the resolution of chromosomal microarray analysis in the prenatal setting affect the rates of pathological and uncertain findings?

1 reference

https://pubmed.ncbi.nlm.nih.gov/24795849

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.7717/PEERJ.354

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

22 August 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q37735343&oldid=2093922891"