(Q50128700)

English

Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype: a cytogenetic risk assessment

scientific article published in July 2005

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/16005334

Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype: a cytogenetic risk assessment (English)

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/16005334

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author name string

Allan Caine

1

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/16005334

A Edna Maltby

2

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/16005334

C Anthony Parkin

3

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/16005334

Jonathan J Waters

4

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/16005334

John A Crolla

5

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/16005334

UK Association of Clinical Cytogeneticists (ACC)

6

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/16005334

language of work or name

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publication date

1 July 2005

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/16005334

number of pages

6

1 reference

based on heuristic

inferred from page(s)

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/16005334

366

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/16005334

9480

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/16005334

123-128

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/16005334

describes a project that uses

fluorescence in situ hybridization

1 reference

based on heuristic

inferred from title

Trisomy in humans: incidence, origin and etiology

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

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Prenatal screening for Down's syndrome with use of maternal serum markers

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Antenatal screening for Down's syndrome.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

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Fetal nuchal translucency: ultrasound screening for chromosomal defects in first trimester of pregnancy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

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UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10–14 weeks of gestation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

based on heuristic

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Integrated screening for Down's syndrome based on tests performed during the first and second trimesters

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

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Screening for chromosomal abnormalities in the first trimester using ultrasound and maternal serum biochemistry in a one-stop clinic: a review of three years prospective experience

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

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Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalities.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

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Defining the efficiency of fluorescence in situ hybridization on uncultured amniocytes on a retrospective cohort of 27407 prenatal diagnoses

1 reference

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7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

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Rapid and simple prenatal DNA diagnosis of Down's syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

based on heuristic

inferred from DOI database lookup

A large-scale evaluation of amnio-PCR for the rapid prenatal diagnosis of fetal trisomy

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Strategies for the rapid prenatal diagnosis of chromosome aneuploidy.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

based on heuristic

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Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR. Assessment on 18,000 consecutive clinical samples.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

based on heuristic

inferred from DOI database lookup

International, collaborative assessment of 146,000 prenatal karyotypes: expected limitations if only chromosome-specific probes and fluorescent in-situ hybridization are used.

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Effectiveness of prenatal chromosomal analysis using multicolour fluorescent in situ hybridisation

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

based on heuristic

inferred from DOI database lookup

An assessment of the use of interphase FISH with chromosome specific probes as an alternative to cytogenetics in prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Confined chorionic mosaicism in prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

based on heuristic

inferred from DOI database lookup

Technical and clinical assessment of fluorescence in situ hybridization: an ACMG/ASHG position statement. I. Technical considerations. Test and Technology Transfer Committee

1 reference

https://api.crossref.org/works/10.1016%2FS0140-6736%2805%2966790-6

7 January 2021

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Identifiers

10.1016/S0140-6736(05)66790-6

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/16005334

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

25 February 2018

http://europepmc.org/abstract/MED/16005334

ResearchGate publication ID

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