Benefits and burdens of using a SNP array in pregnancies at increased risk for the common aneuploidies (Q86279902)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

title

Benefits and burdens of using a SNP array in pregnancies at increased risk for the common aneuploidies (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

author name string

Diane Van Opstal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Femke de Vries

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Lutgarde Govaerts

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Marjan Boter

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Debora Lont

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Stefanie van Veen

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Marieke Joosten

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Karin Diderich

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

Robert-Jan Galjaard

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

publication date

1 March 2015

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

volume

36

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

page(s)

319-326

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

Committee Opinion No. 581: the use of chromosomal microarray analysis in prenatal diagnosis.

25 February 2020

cites work

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Prenatal counseling and the detection of copy-number variants

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Mosaic tetrasomy 5p resulting from an isochromosome 5p marker chromosome: case report and review of literature

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Microarrays as a diagnostic tool in prenatal screening strategies: ethical reflection

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Phenotypic heterogeneity of genomic disorders and rare copy-number variants

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

How does altering the resolution of chromosomal microarray analysis in the prenatal setting affect the rates of pathological and uncertain findings?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Multiplex ligation-dependent probe amplification (MLPA) as a stand-alone test for rapid aneuploidy detection in amniotic fluid cells

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

The future of prenatal diagnosis: rapid testing or full karyotype? An audit of chromosome abnormalities and pregnancy outcomes for women referred for Down's Syndrome testing

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Unexpected findings in cancer predisposition genes detected by array comparative genomic hybridisation: what are the issues?

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Postzygotic isochromosome formation as a cause for false-negative results from chorionic villus chromosome examinations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Towards an evidence-based process for the clinical interpretation of copy number variation

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Estimates of penetrance for recurrent pathogenic copy-number variations

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Prenatal diagnosis using combined quantitative fluorescent polymerase chain reaction and array comparative genomic hybridization analysis as a first-line test: results from over 1000 consecutive cases.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Referral patterns for microarray testing in prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Application of SNP array for rapid prenatal diagnosis: implementation, genetic counselling and diagnostic flow

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Types of array findings detectable in cytogenetic diagnosis: a proposal for a generic classification

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

0.5 Mb array as a first-line prenatal cytogenetic test in cases without ultrasound abnormalities and its implementation in clinical practice

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Recurrent deletions and reciprocal duplications of 10q11.21q11.23 including CHAT and SLC18A3 are likely mediated by complex low-copy repeats

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Implementation of genomic arrays in prenatal diagnosis: the Belgian approach to meet the challenges

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Understanding variable expressivity in microdeletion syndromes.

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Chromosomal microarray versus karyotyping for prenatal diagnosis

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Prenatal diagnosis of chromosomal imbalances

1 reference

https://api.crossref.org/works/10.1002%2FHUMU.22742

7 January 2021

Identifiers

DOI

10.1002/HUMU.22742

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25504762%20AND%20SRC:MED&resulttype=core&format=json

25 February 2020

1 reference