(Q33596140)

English

Prenatal diagnosis from maternal blood: simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sorting

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scholarly article

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Europe PubMed Central

PubMed publication ID

28 July 2017

Prenatal diagnosis from maternal blood: simultaneous immunophenotyping and FISH of fetal nucleated erythrocytes isolated by negative magnetic cell sorting (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

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author name string

Zheng YL

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Carter NP

2

1 reference

Europe PubMed Central

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28 July 2017

Price CM

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Colman SM

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Milton PJ

5

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Hackett GA

6

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Greaves MF

7

1 reference

Europe PubMed Central

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28 July 2017

Ferguson-Smith MA

8

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Europe PubMed Central

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28 July 2017

language of work or name

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publication date

1 December 1993

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Journal of Medical Genetics

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Europe PubMed Central

PubMed publication ID

28 July 2017

30

1 reference

Europe PubMed Central

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28 July 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1051-1056

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Characterization of a cloned repetitive DNA sequence concentrated on the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016647

28 July 2018

Isolation and characterization of a major tandem repeat family from the human X chromosome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016647

28 July 2018

Detection of chromosome aberrations in the human interphase nucleus by visualization of specific target DNAs with radioactive and non-radioactive in situ hybridization techniques: diagnosis of trisomy 18 with probe L1.84.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016647

28 July 2018

Regional assignment of Y-linked DNA probes by deletion mapping and their homology with X-chromosome and autosomal sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016647

28 July 2018

Isolation of fetal DNA from nucleated erythrocytes in maternal blood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016647

28 July 2018

On a non-invasive approach to prenatal diagnosis based on the detection of fetal nucleated cells in maternal blood samples

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016647

28 July 2018

Prenatal diagnosis with repetitive in situ hybridization probes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016647

28 July 2018

Rapid detection of chromosome aneuploidies in uncultured amniocytes by using fluorescence in situ hybridization (FISH)

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016647

28 July 2018

In situ hybridization studies for the detection of common aneuploidies in CVS

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016647

28 July 2018

Simultaneous genotypic and immunophenotypic analysis of interphase cells using dual-color fluorescence: a demonstration of lineage involvement in polycythemia vera.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016647

28 July 2018

Analysis of chromosome 21 copy number in uncultured amniocytes by fluorescence in situ hybridization using a cosmid contig

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016647

28 July 2018

First trimester prenatal diagnosis of trisomy 21 in fetal cells from maternal blood

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016647

28 July 2018

Multicolor fluorescence in situ hybridization for the simultaneous detection of probe sets for chromosomes 13, 18, 21, X and Y in uncultured amniotic fluid cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016647

28 July 2018

Transplacental passage of blood cells

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1016647

28 July 2018

Immunoenzymatic labeling of monoclonal antibodies using immune complexes of alkaline phosphatase and monoclonal anti-alkaline phosphatase (APAAP complexes)

1 reference

https://pubmed.ncbi.nlm.nih.gov/8133505

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Prenatal diagnosis with fetal cells isolated from maternal blood by multiparameter flow cytometry

1 reference

https://pubmed.ncbi.nlm.nih.gov/8133505

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Possible effect of gestational age on the detection of fetal nucleated erythrocytes in maternal blood

1 reference

https://pubmed.ncbi.nlm.nih.gov/8133505

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Fetal cells in the maternal circulation: isolation by multiparameter flow cytometry and confirmation by polymerase chain reaction

1 reference

https://pubmed.ncbi.nlm.nih.gov/8133505

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A degenerate alpha satellite probe, detecting a centromeric deletion on chromosome 21 in an apparently normal human male, shows limitations of the use of satellite DNA probes for interphase ploidy analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/8133505

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Simultaneous fluorescence immunophenotyping and interphase cytogenetics: a contribution to the characterization of tumor cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/8133505

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Combined immunophenotyping and DNA in situ hybridization to study lineage involvement in patients with myelodysplastic syndromes

1 reference

https://pubmed.ncbi.nlm.nih.gov/8133505

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Variations in alphoid DNA sequences escape detection of aneuploidy at interphase by FISH technique

1 reference

https://pubmed.ncbi.nlm.nih.gov/8133505

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

FETAL ERYTHROCYTES IN THE MATERNAL CIRCULATION OF PREGNANT WOMEN

1 reference

https://pubmed.ncbi.nlm.nih.gov/8133505

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1136/JMG.30.12.1051

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

ResearchGate publication ID

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