(Q40269520)

19 September 2017

title

Rapid prenatal diagnosis by QF-PCR: evaluation of 30,000 consecutive clinical samples and future applications (English)

1 reference

19 September 2017

Vincenzo Cirigliano

1

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19 September 2017

Gianfranco Voglino

2

1 reference

19 September 2017

Antonella Marongiu

3

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19 September 2017

Paz Cañadas

4

1 reference

19 September 2017

Elena Ordoñez

5

1 reference

19 September 2017

Elisabet Lloveras

6

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19 September 2017

Alberto Plaja

7

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19 September 2017

Carme Fuster

8

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19 September 2017

Matteo Adinolfi

9

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19 September 2017

language of work or name

English

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publication date

1 September 2006

1 reference

Annals of the New York Academy of Sciences

19 September 2017

published in

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19 September 2017

volume

1075

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19 September 2017

page(s)

288-298

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A prospective comparative study on fluorescence in situ hybridization (FISH) of uncultured amniocytes and standard karyotype analysis.

19 September 2017

cites work

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1368.039

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1368.039

Rapid detection of trisomies 21 and 18 and sexing by quantitative fluorescent multiplex PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1368.039

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1368.039

Rapid detection of aneuploidies by microsatellite and the quantitative fluorescent polymerase chain reaction

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1368.039

Introduction of the QF-PCR analysis for the purposes of prenatal diagnosis in Bulgaria--estimation of applicability of 6 STR markers on chromosomes 21 and 18.

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1368.039

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1368.039

Prenatal diagnosis of common aneuploidies using quantitative fluorescent PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1368.039

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1368.039

Prenatal detection of unbalanced chromosomal rearrangements by array CGH.

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1368.039

Recent advances in fetal nucleic acids in maternal plasma

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1368.039

Increased fetal DNA in the maternal circulation in early pregnancy is associated with an increased risk of preeclampsia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1368.039

Detection of the placental epigenetic signature of the maspin gene in maternal plasma.

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1368.039

Rapid molecular method for prenatal detection of Down's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1196%2FANNALS.1368.039

21 January 2018

Identifiers

DOI

10.1196/ANNALS.1368.039

1 reference

19 September 2017

1 reference