(Q41168788)

English

Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations

scientific article published on 26 November 2010

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

27 September 2017

Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations (English)

1 reference

Europe PubMed Central

27 September 2017

whole genome sequencing

1 reference

based on heuristic

inferred from title

author name string

Paola Evangelidou

1

1 reference

Europe PubMed Central

27 September 2017

Carolina Sismani

2

1 reference

Europe PubMed Central

27 September 2017

Marios Ioannides

3

1 reference

Europe PubMed Central

27 September 2017

Christodoulos Christodoulou

4

1 reference

Europe PubMed Central

27 September 2017

George Koumbaris

5

1 reference

Europe PubMed Central

27 September 2017

Ioannis Kallikas

6

1 reference

Europe PubMed Central

27 September 2017

Ioannis Georgiou

7

1 reference

Europe PubMed Central

27 September 2017

Voula Velissariou

8

1 reference

Europe PubMed Central

27 September 2017

Philippos C Patsalis

9

1 reference

Europe PubMed Central

27 September 2017

language of work or name

1 reference

based on heuristic

inferred from title

publication date

26 November 2010

1 reference

Europe PubMed Central

27 September 2017

Molecular Cytogenetics

1 reference

Europe PubMed Central

27 September 2017

3

1 reference

Europe PubMed Central

27 September 2017

24

1 reference

Europe PubMed Central

27 September 2017

https://scigraph.springernature.com/pub.10.1186/1755-8166-3-24

0 references

Array CGH in patients with learning disability (mental retardation) and congenital anomalies: updated systematic review and meta-analysis of 19 studies and 13,926 subjects

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002366

27 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=3002366

27 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=3002366

27 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=3002366

27 September 2017

Copy number variations and clinical cytogenetic diagnosis of constitutional disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002366

27 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=3002366

27 September 2017

Global variation in copy number in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002366

27 September 2017

Accurate and reliable high-throughput detection of copy number variation in the human genome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002366

27 September 2017

Emerging patterns of cryptic chromosomal imbalance in patients with idiopathic mental retardation and multiple congenital anomalies: a new series of 140 patients and review of published reports

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002366

27 September 2017

A method for accurate detection of genomic microdeletions using real-time quantitative PCR.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002366

27 September 2017

Prenatal diagnosis by array-CGH.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002366

27 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=3002366

27 September 2017

Microarray based comparative genomic hybridisation (array-CGH) detects submicroscopic chromosomal deletions and duplications in patients with learning disability/mental retardation and dysmorphic features

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002366

27 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=3002366

27 September 2017

Microduplication 22q11.2, an emerging syndrome: clinical, cytogenetic, and molecular analysis of thirteen patients

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002366

27 September 2017

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

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002366

27 September 2017

De novo balanced chromosome rearrangements and extra marker chromosomes identified at prenatal diagnosis: clinical significance and distribution of breakpoints

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002366

27 September 2017

Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002366

14 June 2018

A retrospective study by oligonucleotide array-CGH analysis in 50 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=3002366

19 August 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=3002366

19 August 2018

Array-based comparative genomic hybridization analysis of 1176 consecutive clinical genetics investigations.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3002366

19 August 2018

Fluorescence in situ hybridization characterization of apparently balanced translocation reveals cryptic complex chromosomal rearrangements with unexpected level of complexity

1 reference

https://pubmed.ncbi.nlm.nih.gov/21110858

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/21110858

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/21110858

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/21110858

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1186/1755-8166-3-24

1 reference

Europe PubMed Central

27 September 2017

Dimensions Publication ID

0 references

1 reference

Europe PubMed Central

27 September 2017

1 reference

Europe PubMed Central

27 September 2017

ResearchGate publication ID

0 references

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q41168788&oldid=2139099508"