(Q37044378)

English

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

scientific article published on 05 December 2012

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scholarly article

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

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

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

author name string

Francesco Fiorentino

1

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Stefania Napoletano

2

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Fiorina Caiazzo

3

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Mariateresa Sessa

4

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Sara Bono

5

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Letizia Spizzichino

6

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Anthony Gordon

7

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Andrea Nuccitelli

8

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Giuseppe Rizzo

9

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Marina Baldi

10

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

5 December 2012

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

European Journal of Human Genetics

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

21

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

7

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

725-730

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Prenatal chromosomal microarray analysis in a diagnostic laboratory; experience with >1000 cases and review of the literature.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Copy-number changes in prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

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=3722951

29 September 2017

Clinical implementation of whole-genome array CGH as a first-tier test in 5080 pre and postnatal cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Current controversies in prenatal diagnosis 3: is conventional chromosome analysis necessary in the post-array CGH era?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Use of array comparative genomic hybridization for prenatal diagnosis of fetuses with sonographic anomalies and normal metaphase karyotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Array analysis and karyotyping: workflow consequences based on a retrospective study of 36,325 patients with idiopathic developmental delay in the Netherlands

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

High-resolution array genomic hybridization in prenatal diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Pre- and postnatal genetic testing by array-comparative genomic hybridization: genetic counseling perspectives

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

From microscopes to microarrays: dissecting recurrent chromosomal rearrangements

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

The identification of microdeletion syndromes and other chromosome abnormalities: cytogenetic methods of the past, new technologies for the future

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

The discovery of microdeletion syndromes in the post-genomic era: review of the methodology and characterization of a new 1q41q42 microdeletion syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Controversies and challenges of array comparative genomic hybridization in prenatal genetic diagnosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Use of array CGH in the evaluation of dysmorphology, malformations, developmental delay, and idiopathic mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Clinical implementation of chromosomal microarray analysis: summary of 2513 postnatal cases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Evolution of prenatal genetics: from point mutation testing to chromosomal microarray analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Prenatal detection of unbalanced chromosomal rearrangements by array CGH.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Diagnostic genome profiling in mental retardation

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Autosomal dominant inheritance of Williams-Beuren syndrome in a father and son with haploinsufficiency for FKBP6.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Detection of genomic imbalances by array based comparative genomic hybridisation in fetuses with multiple malformations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Array-based comparative genomic hybridization for the genomewide detection of submicroscopic chromosomal abnormalities

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

Essential role of Fkbp6 in male fertility and homologous chromosome pairing in meiosis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

29 September 2017

The introduction of arrays in prenatal diagnosis: a special challenge.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

4 September 2018

Genetic counselling and ethical issues with chromosome microarray analysis in prenatal testing

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

4 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

4 September 2018

Use of array genomic hybridization technology in prenatal diagnosis in Canada.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

4 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

4 September 2018

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

4 September 2018

Diagnostic yield of various genetic approaches in patients with unexplained developmental delay or mental retardation.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

4 September 2018

Targeted genomic microarray analysis for identification of chromosome abnormalities in 1500 consecutive clinical cases.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

4 September 2018

Use of targeted array-based CGH for the clinical diagnosis of chromosomal imbalance: is less more?

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3722951

4 September 2018

Development and validation of a CGH microarray for clinical cytogenetic diagnosis

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.253

21 January 2018

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

1 reference

https://api.crossref.org/works/10.1038%2FEJHG.2012.253

21 January 2018

Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases

1 reference

https://pubmed.ncbi.nlm.nih.gov/23211699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Comparison of microarray-based detection rates for cytogenetic abnormalities in prenatal and neonatal specimens

1 reference

https://pubmed.ncbi.nlm.nih.gov/23211699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ACOG Committee Opinion No. 446: array comparative genomic hybridization in prenatal diagnosis

1 reference

https://pubmed.ncbi.nlm.nih.gov/23211699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Current controversies in prenatal diagnosis 3: For prenatal diagnosis, should we offer less or more than metaphase karyotyping?

1 reference

https://pubmed.ncbi.nlm.nih.gov/23211699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Microarray genetic screening: a prenatal roadblock for life?

1 reference

https://pubmed.ncbi.nlm.nih.gov/23211699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Array comparative genomic hybridization in prenatal diagnosis: another experience

1 reference

https://pubmed.ncbi.nlm.nih.gov/23211699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH

1 reference

https://pubmed.ncbi.nlm.nih.gov/23211699

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1038/EJHG.2012.253

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

Dimensions Publication ID

0 references

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

17 August 2017

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