(Q33635037)

English

Detection of aneuploidy involving chromosomes 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

Detection of aneuploidy involving chromosomes 13, 18, or 21, by fluorescence in situ hybridization (FISH) to interphase and metaphase amniocytes (English)

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

1 reference

based on heuristic

inferred from title

author name string

W L Kuo

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

H Tenjin

2

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

R Segraves

3

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

D Pinkel

4

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

M S Golbus

5

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

J Gray

6

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

language of work or name

0 references

publication date

1 July 1991

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

American Journal of Human Genetics

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

49

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Europe PubMed Central

PubMed publication ID

28 July 2017

1

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

112-119

1 reference

Europe PubMed Central

PubMed publication ID

28 July 2017

describes a project that uses

fluorescence in situ hybridization

1 reference

based on heuristic

inferred from title

Individual interphase chromosome domains revealed by in situ hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683225

21 June 2018

Human chromosome-specific repetitive DNA sequences: novel markers for genetic analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683225

21 June 2018

Rates of mutant and inherited structural cytogenetic abnormalities detected at amniocentesis: results on about 63,000 fetuses.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683225

21 June 2018

Cytogenetic analysis using quantitative, high-sensitivity, fluorescence hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683225

21 June 2018

Detection of chromosome aberrations in metaphase and interphase tumor cells by in situ hybridization using chromosome-specific library probes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683225

21 June 2018

Delineation of individual human chromosomes in metaphase and interphase cells by in situ suppression hybridization using recombinant DNA libraries

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683225

21 June 2018

Detection of chromosome aneuploidy in interphase nuclei from human primary breast tumors using chromosome-specific repetitive DNA probes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683225

21 June 2018

Rapid detection of human chromosome 21 aberrations by in situ hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683225

21 June 2018

Fluorescence in situ hybridization with human chromosome-specific libraries: detection of trisomy 21 and translocations of chromosome 4.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683225

21 June 2018

Maternal age-specific rates for Down syndrome: changes over time.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683225

21 June 2018

Maternal age-specific rates of 47,+21 and other cytogenetic abnormalities diagnosed in the first trimester of pregnancy in chorionic villus biopsy specimens: comparison with rates expected from observations at amniocentesis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683225

21 June 2018

An efficient method for selecting unique-sequence clones from DNA libraries and its application to fluorescent staining of human chromosome 21 using in situ hybridization

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683225

21 June 2018

Maternal serum alpha-fetoprotein and fetal autosomal trisomies

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683225

21 June 2018

Epidemiology of chromosome abnormalities in man

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1683225

21 June 2018

Chromosomal Abnormalities in the Human Population: Estimation of Rates Based on New Haven Newborn Study

1 reference

https://pubmed.ncbi.nlm.nih.gov/2063863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A simple method of reducing the fading of immunofluorescence during microscopy

1 reference

https://pubmed.ncbi.nlm.nih.gov/2063863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

2-Acetylaminofluorene-modified probes for the indirect hybridocytochemical detection of specific nucleic acid sequences

1 reference

https://pubmed.ncbi.nlm.nih.gov/2063863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Maternal age specific rates for chromosome aberrations and factors influencing them: report of a collaborative european study on 52 965 amniocenteses

1 reference

https://pubmed.ncbi.nlm.nih.gov/2063863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Two subsets of human alphoid repetitive DNA show distinct preferential localization in the pericentric regions of chromosomes 13, 18, and 21

1 reference

https://pubmed.ncbi.nlm.nih.gov/2063863

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

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

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