(Q35751507)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

title

Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

author name string

Lluís Armengol

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Julián Nevado

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Clara Serra-Juhé

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Alberto Plaja

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Carmen Mediano

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Fe Amalia García-Santiago

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Manel García-Aragonés

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Olaya Villa

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Elena Mansilla

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Cristina Preciado

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Luis Fernández

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

María Ángeles Mori

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Pablo Daniel Lapunzina

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

Luis Alberto Pérez-Jurado

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

publication date

1 March 2012

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

volume

131

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

page(s)

513-523

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/s00439-011-1095-5

14 February 2020

exact match

0 references

cites work

Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277707

Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277707

Value for money? Array genomic hybridization for diagnostic testing for genetic causes of intellectual disability

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277707

Clinical practice. Prenatal screening for aneuploidy

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277707

Genomic imbalances in neonates with birth defects: high detection rates by using chromosomal microarray analysis.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277707

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

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277707

Economic methods for valuing the outcomes of genetic testing: beyond cost-effectiveness analysis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277707

Molecular cytogenetic and rapid aneuploidy detection methods in prenatal diagnosis

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277707

Economic analyses of human genetics services: a systematic review

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277707

Relative quantification of 40 nucleic acid sequences by multiplex ligation-dependent probe amplification

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277707

The detection of subtelomeric chromosomal rearrangements in idiopathic mental retardation

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277707

Maternal serum screening for Down's syndrome in early pregnancy

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277707

Randomised controlled trial of genetic amniocentesis in 4606 low-risk women

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277707

Estimating a woman's risk of having a pregnancy associated with Down's syndrome using her age and serum alpha-fetoprotein level.

2 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277707

Sensitivity and specificity of screening for Down syndrome with alpha-fetoprotein, hCG, unconjugated estriol, and maternal age.

12 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3277707

Whole-genome microarray analysis in prenatal specimens identifies clinically significant chromosome alterations without increase in results of unclear significance compared to targeted microarray

12 July 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1095-5

Diagnostic utility of array-based comparative genomic hybridization (aCGH) in a prenatal setting.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1095-5

Rapid molecular method for prenatal detection of Down's syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1095-5

Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1095-5

Common recurrent microduplication syndromes: diagnosis and management in clinical practice

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1095-5

Swedish survey on extra structurally abnormal chromosomes in 39 105 consecutive prenatal diagnoses: Prevalence and characterization by fluorescencein situ hybridization

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00439-011-1095-5

Identification of human chromosomes by DNA-binding fluorescent agents

21 January 2018

1 reference

12 December 2020

Sonographic identification of second-trimester fetuses with Down's syndrome

1 reference

12 December 2020

Medical Research Council European trial of chorion villus sampling. MRC working party on the evaluation pf chorion villus sampling

1 reference

12 December 2020

Diagnosis of Down syndrome and other aneuploidies using quantitative polymerase chain reaction and small tandem repeat polymorphisms

1 reference

12 December 2020

Chromosome analysis of human amniotic-fluid cells

1 reference

12 December 2020

10.1007/S00439-011-1095-5

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:21975797%20AND%20SRC:MED&resulttype=core&format=json

14 February 2020

PubMed publication ID

21975797

1 reference