(Q46000499)

English

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.

scientific article

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

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. (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

author name string

F Scott

1

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

K Murphy

2

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

L Carey

3

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

W Greville

4

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

N Mansfield

5

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

P Barahona

6

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

R Robertson

7

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

A McLennan

8

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

publication date

1 May 2013

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

Ultrasound in Obstetrics and Gynecology

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

41

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

5

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

500-507

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

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

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12429

21 January 2018

Applications of array comparative genomic hybridization in obstetrics

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12429

21 January 2018

Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12429

21 January 2018

Microarray comparative genomic hybridization in prenatal diagnosis: a review

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12429

21 January 2018

High-resolution array genomic hybridization in prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12429

21 January 2018

Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12429

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.12429

21 January 2018

Chromosomal microarray versus karyotyping for prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12429

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12429

21 January 2018

Detection of low-level mosaicism and placental mosaicism by oligonucleotide array comparative genomic hybridization.

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12429

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.12429

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.12429

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.12429

21 January 2018

Development and implementation of a new rapid aneuploidy diagnostic service within the UK National Health Service and implications for the future of prenatal diagnosis.

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12429

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12429

21 January 2018

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12429

21 January 2018

Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12429

21 January 2018

Increased nuchal translucency with normal karyotype: a follow-up study of 100 cases supplemented with CGH and MLPA analyses.

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12429

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1002%2FUOG.12429

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.12429

21 January 2018

Identifiers

10.1002/UOG.12429

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 December 2017

http://europepmc.org/abstract/MED/23401365

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=Q46000499&oldid=905709857"