Clinical utility of noninvasive fetal trisomy (NIFTY) test--early experience. (Q36353229)

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27 January 2020

title

Clinical utility of noninvasive fetal trisomy (NIFTY) test--early experience (English)

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1

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author name string

Mei Ki Chan

2

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27 January 2020

Pui Shan Salome Lo

3

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Hon Yee Connie Chan

4

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Wai Sze Kim Chan

5

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Tik Yee Koo

6

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Hoi Yan Joyce Ng

7

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Ritsuko K Pooh

8

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publication date

28 April 2012

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Journal of Maternal-Fetal and Neonatal Medicine

27 January 2020

published in

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volume

25

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issue

10

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page(s)

1856-1859

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DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study

27 January 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3483059

Prenatal Detection of Down Syndrome using Massively Parallel Sequencing (MPS): a rapid response statement from a committee on behalf of the Board of the International Society for Prenatal Diagnosis, 24 October 2011.

30 September 2017

1 reference

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Noninvasive prenatal diagnosis: pregnant women's interest and expected uptake

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3483059

Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing

30 September 2017

1 reference

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Screening for fetal aneuploidies at 11 to 13 weeks

30 September 2017

1 reference

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Pregnant women's responses to information about an increased risk of carrying a baby with Down syndrome

30 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3483059

Noninvasive prenatal diagnosis of common fetal chromosomal aneuploidies by maternal plasma DNA sequencing.

30 September 2017

1 reference

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Optimal detection of fetal chromosomal abnormalities by massively parallel DNA sequencing of cell-free fetal DNA from maternal blood

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3483059

First trimester combined screening for Trisomy 21 in Hong Kong: outcome of the first 10,000 cases.

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3483059

Presence of fetal DNA in maternal plasma and serum

22 September 2018

1 reference

Crossref

https://api.crossref.org/works/10.3109%2F14767058.2012.678442

Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype

21 January 2018

1 reference

Crossref

https://api.crossref.org/works/10.3109%2F14767058.2012.678442

Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22471583

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.3109/14767058.2012.678442

1 reference

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27 January 2020

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27 January 2020

PubMed publication ID

22471583

1 reference

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