(Q30414408)

English

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

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

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

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Stanley F Nelson

11

object named as

Stanley F Nelson

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

author name string

Glenn E Palomaki

1

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Cosmin Deciu

2

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Edward M Kloza

3

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Geralyn M Lambert-Messerlian

4

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

James E Haddow

5

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Louis M Neveux

6

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Mathias Ehrich

7

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Dirk van den Boom

8

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Allan T Bombard

9

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Wayne W Grody

10

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Jacob A Canick

12

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

language of work or name

0 references

publication date

2 February 2012

1 reference

Europe PubMed Central

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21 August 2017

Genetics in Medicine

1 reference

Europe PubMed Central

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21 August 2017

14

1 reference

Europe PubMed Central

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21 August 2017

3

1 reference

Europe PubMed Central

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21 August 2017

296-305

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3938175

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3938175

20 June 2018

Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3938175

20 June 2018

Maternal plasma DNA analysis with massively parallel sequencing by ligation for noninvasive prenatal diagnosis of trisomy 21.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3938175

20 June 2018

The maternal age-specific live birth prevalence of trisomies 13 and 18 compared to trisomy 21 (Down syndrome).

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3938175

20 June 2018

Personalized copy number and segmental duplication maps using next-generation sequencing.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3938175

20 June 2018

Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3938175

20 June 2018

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3938175

20 June 2018

Patterns of first-year survival among infants with selected congenital anomalies in Texas, 1995-1997.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3938175

20 June 2018

Randomised controlled trial of genetic amniocentesis in 4606 low-risk women

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3938175

20 June 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3938175

20 June 2018

Prospective intervention trial of a screening protocol to identify fetal trisomy 18 using maternal serum alpha‐fetoprotein, unconjugated oestriol, and human chorionic gonadotropin

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3938175

20 June 2018

Population-based analyses of mortality in trisomy 13 and trisomy 18.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.73

21 January 2018

Risk-based prenatal screening for trisomy 18 using alpha-fetoprotein, unconjugated oestriol and human chorionic gonadotropin.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.73

21 January 2018

Maternal serum-integrated screening for trisomy 18 using both first- and second-trimester markers

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.73

21 January 2018

Screening for trisomy 18 by fetal nuchal translucency and maternal serum free beta-hCG and PAPP-A at 10-14 weeks of gestation.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.73

21 January 2018

Evidence-based obstetric ethics and informed decision-making by pregnant women about invasive diagnosis after first-trimester assessment of risk for trisomy 21.

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.73

21 January 2018

The risk of fetal loss following a prenatal diagnosis of trisomy 13 or trisomy 18

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.73

21 January 2018

Executive summary

1 reference

https://api.crossref.org/works/10.1038%2FGIM.2011.73

21 January 2018

ACOG Practice Bulletin No. 88, December 2007. Invasive prenatal testing for aneuploidy

1 reference

https://pubmed.ncbi.nlm.nih.gov/22281937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/22281937

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/GIM.2011.73

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

21 August 2017

ResearchGate publication ID

0 references

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