(Q41809147)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22413963%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

title

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities (English)

1 reference

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25 January 2020

1

1 reference

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25 January 2020

author name string

Marjan Boter

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22413963%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

Gretel O Oudesluijs

3

1 reference

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25 January 2020

Titia Cohen-Overbeek

4

1 reference

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25 January 2020

Lutgarde Cp Govaerts

5

1 reference

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25 January 2020

Karin Em Diderich

6

1 reference

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25 January 2020

Renske Oegema

7

1 reference

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25 January 2020

Maarten Fcm Knapen

8

1 reference

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25 January 2020

Ingrid Mbh van de Laar

9

1 reference

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25 January 2020

Marieke Joosten

10

1 reference

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25 January 2020

Diane Van Opstal

11

1 reference

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25 January 2020

Robert-Jan H Galjaard

12

1 reference

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25 January 2020

publication date

13 March 2012

1 reference

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25 January 2020

published in

Molecular Cytogenetics

1 reference

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25 January 2020

volume

5

1 reference

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25 January 2020

page(s)

14

1 reference

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25 January 2020

issue

1

1 reference

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https://scigraph.springernature.com/pub.10.1186/1755-8166-5-14

25 January 2020

exact match

0 references

cites work

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3328283

A fast and accurate method to detect allelic genomic imbalances underlying mosaic rearrangements using SNP array data

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3328283

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

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3328283

Mechanisms of mosaicism, chimerism and uniparental disomy identified by single nucleotide polymorphism array analysis

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3328283

Visualization of shared genomic regions and meiotic recombination in high-density SNP data

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3328283

Clinical use of array comparative genomic hybridization (aCGH) for prenatal diagnosis in 300 cases

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3328283

Prenatal detection of unbalanced chromosomal rearrangements by array CGH.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3328283

Outcome of cases of de novo structural rearrangements diagnosed at amniocentesis

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3328283

Exclusion of chromosomal mosaicism: tables of 90%, 95% and 99% confidence limits and comments on use

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3328283

Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: a cohort study of 3171 pregnancies.

6 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3328283

Whole-genome array CGH identifies pathogenic copy number variations in fetuses with major malformations and a normal karyotype.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3328283

Understanding variable expressivity in microdeletion syndromes.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3328283

A retrospective study by oligonucleotide array-CGH analysis in 50 fetuses with multiple malformations.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3328283

High resolution array analysis: diagnosing pregnancies with abnormal ultrasound findings.

18 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3328283

Twenty years of experience in advanced ultrasound scanning for fetal anomalies in Rotterdam

18 August 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/22413963

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1186/1755-8166-5-14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22413963%20AND%20SRC:MED&resulttype=core&format=json

Dimensions Publication ID

25 January 2020

1028955299

0 references

Fatcat ID

release_kuxhdvbhlbakpovdxwb4to24qi

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/kuxhdvbhlbakpovdxwb4to24qi

mapped directly with Wikidata item

24 November 2022

based on heuristic

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22413963%20AND%20SRC:MED&resulttype=core&format=json

25 January 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22413963%20AND%20SRC:MED&resulttype=core&format=json