(Q37933548)

25 August 2017

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title

Use of a DNA method, QF-PCR, in the prenatal diagnosis of fetal aneuploidies (English)

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25 August 2017

Sylvie Langlois

1

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25 August 2017

Alessandra Duncan

series ordinal

2

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25 August 2017

publication date

1 September 2011

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Journal of Obstetrics and Gynaecology Canada

25 August 2017

published in

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25 August 2017

volume

33

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25 August 2017

issue

9

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25 August 2017

page(s)

955-960

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New molecular techniques for the prenatal detection of chromosomal aneuploidy.

25 August 2017

cites work

1 reference

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7 January 2021

An algorithm for the prenatal detection of chromosome anomalies by QF-PCR and G-banded analysis.

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7 January 2021

The introduction of QF-PCR in prenatal diagnosis of fetal aneuploidies: time for reconsideration

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7 January 2021

Ultrasound findings before amniocentesis in selecting the method of analysing the sample.

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7 January 2021

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

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7 January 2021

Detection of aneuploidy in chromosomes X, Y, 13, 18 and 21 by QF-PCR in 662 selected pregnancies at risk

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7 January 2021

Strategies for the rapid prenatal diagnosis of chromosome aneuploidy.

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7 January 2021

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.

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7 January 2021

Validation of QF-PCR for prenatal aneuploidy screening in the United States.

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Quantitative fluorescent polymerase chain reaction versus cytogenetics: risk-related indication and clinical implication of nondetected chromosomal disorders

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7 January 2021

Rapid prenatal diagnosis of common aneuploidies in amniotic fluid using quantitative fluorescent polymerase chain reaction.

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7 January 2021

QF-PCR-based prenatal detection of common aneuploidies in the Czech population: five years of experience.

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7 January 2021

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7 January 2021

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7 January 2021

Frequencies of chromosomal abnormalities at amniocentesis: over 20 years of cytogenetic analyses in one laboratory

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7 January 2021

Karyotypes found in the population declared at increased risk of Down syndrome following maternal serum screening

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7 January 2021

Suitability of rapid aneuploidy detection for prenatal diagnosis

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7 January 2021

Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis

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7 January 2021

Comparison of multiplex ligation-dependent probe amplification and karyotyping in prenatal diagnosis

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7 January 2021

Rapid and novel prenatal molecular assay for detecting aneuploidies and microdeletion syndromes

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7 January 2021

10.1016/S1701-2163(16)35022-8

Identifiers

DOI

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