(Q34042854)

English

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

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

1 reference

based on heuristic

inferred from title

author name string

Ti-Zhen Yan

1

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Qiu-Hua Mo

2

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Ren Cai

3

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Xue Chen

4

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Cui-Mei Zhang

5

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Yan-Hui Liu

6

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Ya-Jun Chen

7

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Wan-Jun Zhou

8

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Fu Xiong

9

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

Xiang-Min Xu

10

1 reference

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PubMed publication ID

30 July 2017

language of work or name

0 references

publication date

29 September 2011

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

9

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

e24779

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

copyright license

Creative Commons Attribution 4.0 International

29 September 2011

1 reference

April 2022 Public Data File from Crossref

copyright status

0 references

Alpha thalassemia major--new mutations, intrauterine management, and outcomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182989

5 July 2018

Size fractionation of cell-free DNA in maternal plasma improves the detection of a paternally inherited beta-thalassemia point mutation by MALDI-TOF mass spectrometry

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182989

5 July 2018

Detection of circulating fetal nucleic acids: a review of methods and applications

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182989

5 July 2018

Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on 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=3182989

5 July 2018

The use of cell-free fetal nucleic acids in maternal blood for non-invasive prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182989

5 July 2018

Global epidemiology of haemoglobin disorders and derived service indicators

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182989

5 July 2018

Microsatellite markers within --SEA breakpoints for prenatal diagnosis of HbBarts hydrops fetalis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182989

5 July 2018

Non-invasive prenatal detection of achondroplasia in size-fractionated cell-free DNA by MALDI-TOF MS assay

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182989

5 July 2018

Alpha-thalassemia: Hb H disease and Hb Barts hydrops fetalis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182989

5 July 2018

MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182989

5 July 2018

Prenatal diagnosis using fetal cells and cell-free fetal DNA in maternal blood: what is currently feasible?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3182989

5 July 2018

Simple non-invasive prenatal detection of Hb Bart's disease by analysis of fetal erythrocytes in maternal blood.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024779

21 January 2018

Noninvasive prenatal diagnosis for hemoglobin Bart's hydrops fetalis.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024779

21 January 2018

Development and application of a real-time quantitative PCR for prenatal detection of fetal alpha(0)-thalassemia from maternal plasma.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024779

21 January 2018

Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024779

21 January 2018

Peptide-nucleic acid-mediated enriched polymerase chain reaction as a key point for non-invasive prenatal diagnosis of beta-thalassemia.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024779

21 January 2018

Fetal DNA: strategies for optimal recovery

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024779

21 January 2018

Accurate and robust quantification of circulating fetal and total DNA in maternal plasma from 5 to 41 weeks of gestation.

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024779

21 January 2018

Size separation of circulatory DNA in maternal plasma permits ready detection of fetal DNA polymorphisms

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024779

21 January 2018

Presence of fetal DNA in maternal plasma and serum

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024779

21 January 2018

Prenatal exclusion of β thalassaemia major by examination of maternal plasma

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0024779

21 January 2018

Noninvasive prenatal exclusion of haemoglobin Bart's using foetal DNA from maternal plasma

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980356

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980356

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[Rapid detection of alpha-thalassemia of Southeast Asian deletion by polymerase chain reaction and its application to prenatal diagnosis]

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980356

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Noninvasive prenatal exclusion of congenital adrenal hyperplasia by maternal plasma analysis: a feasibility study

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980356

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Intact fetal cells in maternal plasma: are they really there?

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980356

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cell-free fetal DNA in maternal blood: evolving clinical applications

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980356

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Improvement in sensitivity of allele-specific PCR facilitates reliable noninvasive prenatal detection of cystic fibrosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980356

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A randomized comparison of transcervical and transabdominal chorionic-villus sampling. The U.S. National Institute of Child Health and Human Development Chorionic-Villus Sampling and Amniocentesis Study Group

1 reference

https://pubmed.ncbi.nlm.nih.gov/21980356

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1371/JOURNAL.PONE.0024779

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

2011PLoSO...624779Y

0 references

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

30 July 2017

ResearchGate publication ID

0 references

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