(Q35088343)

6 August 2017

title

Whole-genome array CGH evaluation for replacing prenatal karyotyping in Hong Kong (English)

1 reference

6 August 2017

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whole genome sequencing

1 reference

Anita S Y Kan

1

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6 August 2017

Elizabeth T Lau

2

1 reference

6 August 2017

W F Tang

3

1 reference

6 August 2017

Sario S Y Chan

4

1 reference

6 August 2017

Simon C K Ding

5

1 reference

6 August 2017

Kelvin Y K Chan

6

1 reference

6 August 2017

C P Lee

7

1 reference

6 August 2017

Pui Wah Hui

8

1 reference

6 August 2017

Brian H Y Chung

9

1 reference

6 August 2017

K Y Leung

10

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6 August 2017

Teresa Ma

11

1 reference

6 August 2017

Wing C Leung

12

1 reference

6 August 2017

Mary H Y Tang

13

1 reference

6 August 2017

language of work or name

English

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publication date

5 February 2014

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6 August 2017

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6 August 2017

volume

9

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6 August 2017

issue

2

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6 August 2017

page(s)

e87988

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Creative Commons Attribution 4.0 International

6 August 2017

copyright license

start time

5 February 2014

1 reference

April 2022 Public Data File from Crossref

copyright status

copyrighted

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cites work

The clinical utility of microarray technologies applied to prenatal cytogenetics in the presence of a normal conventional karyotype: a 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=3914896

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

Use of prenatal chromosomal microarray: prospective cohort study and systematic review and meta-analysis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

Chromosomal microarray versus karyotyping for prenatal diagnosis

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

Integration of microarray technology into prenatal diagnosis: counselling issues generated during the NICHD clinical trial

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

QF-PCR: application, overview and review of the literature

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

Microarray application in prenatal diagnosis: a position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

Array-based technology and recommendations for utilization in medical genetics practice for detection of chromosomal abnormalities

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

QF-PCR as a stand-alone test for prenatal samples: the first 2 years' experience in the London region

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

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

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

The inv dup (15) or idic (15) syndrome (Tetrasomy 15q)

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

Chromosome 15q11-13 duplication syndrome brain reveals epigenetic alterations in gene expression not predicted from copy number.

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia

8 July 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

High resolution comparative genomic hybridisation in clinical cytogenetics

8 July 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0087988

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0087988

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0087988

Assessing discrepant findings between QF-PCR on uncultured prenatal samples and karyotyping on long-term culture.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0087988

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.

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0087988

Defining the impact of maternal cell contamination on the interpretation of prenatal microarray analysis

21 January 2018

1 reference

https://api.crossref.org/works/10.1371%2FJOURNAL.PONE.0087988

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

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

Two unusual cases of haemoglobin Bart's hydrops fetalis due to uniparental disomy or non-paternity.

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

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

27 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3914896

Recurrent rearrangements in the proximal 15q11–q14 region: a new breakpoint cluster specific to unbalanced translocations

27 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/24505343

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1371/JOURNAL.PONE.0087988

1 reference

release_emus3xcd6rhzljjhfwi6p75pue

6 August 2017

0 references

1 reference

Fatcat

https://api.fatcat.wiki/v0/release/emus3xcd6rhzljjhfwi6p75pue

mapped directly with Wikidata item

24 November 2022

based on heuristic

PMC publication ID

3914896

1 reference

6 August 2017

1 reference