(Q34312211)

1 August 2017

title

Recent advances in the prenatal interrogation of the human fetal genome (English)

1 reference

1 August 2017

Lisa Hui

1

0 references

Diana W. Bianchi

series ordinal

2

object named as

Diana W Bianchi

1 reference

1 August 2017

publication date

15 November 2012

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1 August 2017

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1 August 2017

volume

29

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1 August 2017

issue

2

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1 August 2017

page(s)

84-91

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Evaluation of a novel assay for detection of the fetal marker RASSF1A: facilitating improved diagnostic reliability of noninvasive prenatal diagnosis

1 August 2017

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Non-invasive prenatal measurement of the fetal genome

6 July 2018

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Noninvasive whole-genome sequencing of a human fetus.

6 July 2018

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Noninvasive prenatal diagnosis empowered by high-throughput sequencing

6 July 2018

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Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trial

6 July 2018

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Genomic microarrays: a technology overview

6 July 2018

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Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18.

6 July 2018

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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

6 July 2018

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6 July 2018

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Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011

6 July 2018

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

6 July 2018

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

6 July 2018

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

6 July 2018

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

6 July 2018

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Noninvasive fetal genotyping of human platelet antigen-1a

6 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

Noninvasive fetal blood group genotyping of rhesus D, c, E and of K in alloimmunised pregnant women: evaluation of a 7-year clinical experience

6 July 2018

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Prenatal, noninvasive and preimplantation genetic diagnosis of inherited disorders: hemoglobinopathies

6 July 2018

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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

Noninvasive prenatal diagnosis of hemophilia by microfluidics digital PCR analysis of maternal plasma DNA.

6 July 2018

1 reference

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

6 July 2018

1 reference

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Whole-genome molecular haplotyping of single cells

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

Non-invasive prenatal determination of fetal sex: translating research into clinical practice

6 July 2018

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Additional information from array comparative genomic hybridization technology over conventional karyotyping in prenatal diagnosis: a systematic review and meta-analysis

6 July 2018

1 reference

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QF-PCR as a stand-alone test for prenatal samples: the first 2 years' experience in the London region

6 July 2018

1 reference

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Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

6 July 2018

1 reference

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High-resolution array genomic hybridization in prenatal diagnosis

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

Microfluidics digital PCR reveals a higher than expected fraction of fetal DNA in maternal plasma

6 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

Chorionic villus sampling and amniocentesis in 2008.

6 July 2018

1 reference

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Digital PCR for the molecular detection of fetal chromosomal aneuploidy

6 July 2018

1 reference

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Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis

6 July 2018

1 reference

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ACOG Practice Bulletin No. 77: Screening for Fetal Chromosomal Abnormalities

6 July 2018

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Prediction of fetal D status from maternal plasma: introduction of a new noninvasive fetal RHD genotyping service

6 July 2018

1 reference

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Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data. National Institute of Child Health and Development Fetal Cell Isolation Study.

6 July 2018

1 reference

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

6 July 2018

1 reference

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

The introduction of arrays in prenatal diagnosis: a special challenge.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

Single molecule sequencing of free DNA from maternal plasma for noninvasive trisomy 21 detection.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

Early non-invasive detection of fetal Y chromosome sequences in maternal plasma using multiplex PCR.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

Report of the first nationally implemented clinical routine screening for fetal RHD in D- pregnant women to ascertain the requirement for antenatal RhD prophylaxis

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR, results of 9 years of clinical experience.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

Detection of aneuploidy with digital polymerase chain reaction.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

Hypermethylated RASSF1A in maternal plasma: A universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

At-home fetal DNA gender testing: caveat emptor.

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

First-trimester or second-trimester screening, or both, for Down's syndrome

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

Non-invasive prenatal screening of fetal sex chromosomal abnormalities: perspective of pregnant women

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

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

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

First and second trimester antenatal screening for Down's syndrome: the results of the Serum, Urine and Ultrasound Screening Study (SURUSS)

28 October 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4378900

Chromosome analysis of human amniotic-fluid cells

28 October 2018

1 reference

12 December 2020

Intrauterine diagnosis and management of genetic defects

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

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

1 reference

12 December 2020

Noninvasive prenatal genetic testing for fetal aneuploidy detects maternal trisomy X

1 reference

12 December 2020

Prenatal diagnosis of Down's syndrome

1 reference

12 December 2020

Presence of fetal DNA in maternal plasma and serum

1 reference

12 December 2020

UK multicentre project on assessment of risk of trisomy 21 by maternal age and fetal nuchal-translucency thickness at 10–14 weeks of gestation

1 reference

12 December 2020

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

1 reference

12 December 2020

ACOG Committee Opinion No. 446: array comparative genomic hybridization in prenatal diagnosis

1 reference

12 December 2020

First-trimester prenatal diagnosis performed on pregnant women with fetal ultrasound abnormalities: the reliability of interphase fluorescence in situ hybridization (FISH) on mesenchymal core for the main aneuploidies

1 reference

12 December 2020

ThalassoChip, an array mutation and single nucleotide polymorphism detection tool for the diagnosis of β-thalassaemia

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

10.1016/J.TIG.2012.10.013

Identifiers

DOI

1 reference

release_df6zs43c4bfsbomzub7rvqwqqe

1 August 2017

Fatcat ID

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/df6zs43c4bfsbomzub7rvqwqqe

24 November 2022

mapped directly with Wikidata item

PMC publication ID

4378900

1 reference

1 August 2017

1 reference