(Q26827338)

language of work or name

1 reference

21 May 2014

1 reference

Journal of Clinical Medicine

published in

1 reference

volume

3

1 reference

issue

2

1 reference

page(s)

537-65

1 reference

Creative Commons Attribution 4.0 International

copyright license

start time

21 May 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

0 references

cites work

DNA Sequencing versus Standard Prenatal Aneuploidy Screening

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy

7 April 2017

1 reference

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Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Update on Procedure-Related Risks for Prenatal Diagnosis Techniques

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

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

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Prenatal Diagnosis of Fetal RhD Status by Molecular Analysis of Maternal Plasma

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohort

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Turner syndrome revisited: review of new data supports the hypothesis that all viable 45,X cases are cryptic mosaics with a rescue cell line, implying an origin by mitotic loss

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Noninvasive prenatal diagnosis in a fetus at risk for methylmalonic acidemia

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Fetal fraction estimate in twin pregnancies using directed cell-free DNA analysis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Assessment of fetal sex chromosome aneuploidy using directed cell-free DNA analysis.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Obstetricians and gynecologists' practice and opinions of expanded carrier testing and noninvasive prenatal testing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Maternal mosaicism is a significant contributor to discordant sex chromosomal aneuploidies associated with noninvasive prenatal testing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Impact of prenatal technologies on the sex ratio in India: an overview

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Prenatal detection of fetal triploidy from cell-free DNA testing in maternal blood

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Non-invasive prenatal testing for fetal sex determination: is ultrasound still relevant?

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Noninvasive prenatal detection for pathogenic CNVs: the application in α-thalassemia

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Non-invasive prenatal testing for aneuploidy: current status and future prospects

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Noninvasive prenatal molecular karyotyping from maternal plasma

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress made

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Initial clinical laboratory experience in noninvasive prenatal testing for fetal aneuploidy from maternal plasma DNA samples

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Gestational age and maternal weight effects on fetal cell-free DNA in maternal plasma

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Clinical experience of noninvasive prenatal testing with cell-free DNA for fetal trisomies 21, 18, and 13, in a general screening population

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Current status in non-invasive prenatal detection of Down syndrome, trisomy 18, and trisomy 13 using cell-free DNA in maternal plasma

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Safe, accurate, prenatal diagnosis of thanatophoric dysplasia using ultrasound and free fetal DNA.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Clinical utility and cost of non-invasive prenatal testing with cfDNA analysis in high-risk women based on a US population

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasma

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

The fetal fraction of cell-free DNA in maternal plasma is not affected by a priori risk of fetal trisomy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Noninvasive prenatal diagnosis of monogenic diseases by targeted massively parallel sequencing of maternal plasma: application to β-thalassemia.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

From prenatal genomic diagnosis to fetal personalized medicine: progress and challenges

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Non-invasive prenatal measurement of the fetal genome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

A multifactorial relationship exists between total circulating cell-free DNA levels and maternal BMI

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Noninvasive whole-genome sequencing of a human fetus.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Noninvasive prenatal diagnosis of monogenic disorders

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Digital PCR analysis of maternal plasma for noninvasive detection of sickle cell anemia

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Noninvasive prenatal diagnosis of a fetal microdeletion syndrome

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Reliable detection of paternal SNPs within deletion breakpoints for non-invasive prenatal exclusion of homozygous α-thalassemia in maternal plasma

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Noninvasive fetal sex determination using cell-free fetal DNA: a systematic review and meta-analysis

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

New aids for the non-invasive prenatal diagnosis of achondroplasia: dysmorphic features, charts of fetal size and molecular confirmation using cell-free fetal DNA in maternal plasma.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Targeted massively parallel sequencing of maternal plasma DNA permits efficient and unbiased detection of fetal alleles

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Non-invasive aneuploidy detection using free fetal DNA and RNA in maternal plasma: recent progress and future possibilities

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Relationships Between Cell-Free DNA and Serum Analytes in the First and Second Trimesters of Pregnancy

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Sites of differential DNA methylation between placenta and peripheral blood: molecular markers for noninvasive prenatal diagnosis of aneuploidies

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Incidence of non-age-dependent chromosomal abnormalities: a population-based study on 88965 amniocenteses.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

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

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Improvement in strategies for the non-invasive prenatal diagnosis of Huntington disease

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

RHD genotyping from maternal plasma: guidelines and technical challenges

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Persistent gestational trophoblastic neoplasia after partial hydatidiform mole incidence and outcome.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Second trimester maternal serum analytes in triploid pregnancies: correlation with phenotype and sex chromosome complement

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Rapid clearance of fetal DNA from maternal plasma

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis.

28 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Free fetal DNA in maternal plasma in anembryonic pregnancies: confirmation that the origin is the trophoblast.

28 September 2017

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Huntington disease-unaffected fetus diagnosed from maternal plasma using QF-PCR.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Noninvasive prenatal diagnosis of early onset primary dystonia I in maternal plasma

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Non-invasive prenatal diagnosis of beta-thalassemia and sickle-cell disease using pyrophosphorolysis-activated polymerization and melting curve analysis.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Prenatal technologies and the sex ratio.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Noninvasive prenatal testing for early sex identification: a few benefits and many concerns

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

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

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Non-invasive prenatal testing of fetal whole chromosome aneuploidy by massively parallel sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Diagnostic accuracy of random massively parallel sequencing for non-invasive prenatal detection of common autosomal aneuploidies: a collaborative study in Europe.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Trisomy 13 detection in the first trimester of pregnancy using a chromosome-selective cell-free DNA analysis method.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Implementation of maternal blood cell-free DNA testing in early screening for aneuploidies.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Noninvasive prenatal detection of sex chromosomal aneuploidies by sequencing circulating cell-free DNA from maternal plasma

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

DNA sequencing of maternal plasma to identify Down syndrome and other trisomies in multiple gestations

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Non-invasive prenatal screening of fetal Down syndrome by maternal plasma DNA sequencing in twin pregnancies

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Cell-free DNA analysis for trisomy risk assessment in first-trimester twin pregnancies.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Circulating fetal cell-free DNA fractions differ in autosomal aneuploidies and monosomy X.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Still a screening test: more attention needed to noninvasive prenatal test false-positive rates

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Is it time to sound an alarm about false-positive cell-free DNA testing for fetal aneuploidy?

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Theoretical performance of non-invasive prenatal testing for chromosome imbalances using counting of cell-free DNA fragments in maternal plasma.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

The impact of maternal plasma DNA fetal fraction on next generation sequencing tests for common fetal aneuploidies.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Discordant results between fetal karyotyping and non-invasive prenatal testing by maternal plasma sequencing in a case of uniparental disomy 21 due to trisomic rescue.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Discordant noninvasive prenatal testing results in a patient subsequently diagnosed with metastatic disease

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Non-invasive prenatal diagnosis for Down syndrome: the paradigm will shift, but slowly.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Noninvasive prenatal testing for fetal aneuploidy: clinical assessment and a plea for restraint

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

NSGC practice guideline: prenatal screening and diagnostic testing options for chromosome aneuploidy

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Maternal cfDNA screening for Down syndrome--a cost sensitivity analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

First-trimester contingent screening for trisomy 21 by biomarkers and maternal blood cell-free DNA testing

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

First-trimester contingent screening for trisomies 21, 18 and 13 by biomarkers and maternal blood cell-free DNA testing.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

First-trimester Down syndrome screening using additional serum markers with and without nuchal translucency and cell-free DNA.

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Methods to Increase the Percentage of Free Fetal DNA Recovered From the Maternal Circulation

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Detection of microdeletion 22q11.2 in a fetus by next-generation sequencing of maternal plasma

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Presence of fetal DNA in maternal plasma and serum

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Maternal Plasma DNA Sequencing Reveals the Genome-Wide Genetic and Mutational Profile of the Fetus

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

A robust second-generation genome-wide test for fetal aneuploidy based on shotgun sequencing cell-free DNA in maternal blood

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Secondary findings from non-invasive prenatal testing for common fetal aneuploidies by whole genome sequencing as a clinical service

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

Two cases of placental T21 mosaicism: challenging the detection limits of non-invasive prenatal testing

21 January 2018

1 reference

https://api.crossref.org/works/10.3390%2FJCM3020537

No evidence of fetal DNA persistence in maternal plasma after pregnancy

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4449688

Noninvasive prenatal genetic testing for fetal aneuploidy detects maternal trisomy X

28 November 2018

1 reference

12 December 2020

Detection of fetal RHD-specific sequences in maternal plasma

1 reference

12 December 2020

Prenatal DNA diagnosis of a single-gene disorder from maternal plasma

1 reference

12 December 2020

Fetal Fraction in Maternal Plasma Cell-Free DNA at 11–13 Weeks’ Gestation: Effect of Maternal and Fetal Factors

1 reference

12 December 2020

Cytogenetic results from the U.S. Collaborative Study on CVS

1 reference

12 December 2020

Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma

1 reference

12 December 2020

Placental volume measured by three-dimensional ultrasound at 11 to 13 + 6 weeks of gestation: relation to chromosomal defects

1 reference

12 December 2020

Noninvasive prenatal testing of fetal aneuploidies by massively parallel sequencing in a prospective Chinese population

1 reference

12 December 2020

Chromosome-selective sequencing of maternal plasma cell–free DNA for first-trimester detection of trisomy 21 and trisomy 18

1 reference

12 December 2020

Noninvasive prenatal testing of trisomies 21 and 18 by massively parallel sequencing of maternal plasma DNA in twin pregnancies

1 reference

12 December 2020

A new era in noninvasive prenatal testing

1 reference

12 December 2020

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

1 reference

12 December 2020

Effect of labor on postpartum clearance of cell-free fetal DNA from the maternal circulation

1 reference

12 December 2020

Clinical utility and cost of non-invasive prenatal testing

1 reference

12 December 2020

Noninvasive prenatal testing for fetal trisomies in a routinely screened first-trimester population

1 reference

12 December 2020

European non-invasive trisomy evaluation (EU-NITE) study: a multicenter prospective cohort study for non-invasive fetal trisomy 21 testing

1 reference

12 December 2020

Non-invasive prenatal diagnosis of single-gene disorders from maternal blood

1 reference

12 December 2020

Committee Opinion No. 545: Noninvasive prenatal testing for fetal aneuploidy

1 reference

12 December 2020

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

1 reference

12 December 2020

Identifiers

0 references

1 reference

PubMed publication ID

26237390

1 reference