(Q24606043)

2

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Mindy P Dabell

3

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Justine Coppinger

4

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Anne M Bandholz

5

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Jay W Ellison

6

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J Britt Ravnan

7

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Beth S Torchia

8

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Blake C Ballif

9

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Allan J Fisher

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

10

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language of work or name

English

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publication date

October 2012

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published in

Prenatal Diagnosis

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volume

32

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issue

10

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page(s)

986-95

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cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

Experience with microarray-based comparative genomic hybridization for prenatal diagnosis in over 5000 pregnancies

7 April 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

Detection of chromosome aberrations in the second trimester using genetic amniocentesis: experience during 1995-2004.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

ACOG Practice Bulletin No. 77: Screening for Fetal Chromosomal Abnormalities

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

Prospective ranking of the sonographic markers for aneuploidy: data of 2143 prenatal cytogenetic diagnoses referred for abnormalities on ultrasound.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

Ultrasound screening for fetal chromosome anomalies

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

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

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

Ultrasonographically detectable markers of fetal chromosomal abnormalities

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

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

30 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

Identification of clinically significant, submicroscopic chromosome alterations and UPD in fetuses with ultrasound anomalies using genome-wide 250k SNP array analysis

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

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

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

Changes in the utilization of prenatal diagnosis

28 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=3509216

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

28 November 2018

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Prenatal ultrasound detection of talipes equinovarus in a non-selected population of 49 314 deliveries in Norway

1 reference

12 December 2020

Should determination of the karyotype be systematic for all malformations detected by obstetrical ultrasound?

1 reference

12 December 2020

Array comparative genomic hybridization in prenatal diagnosis: another experience

1 reference

12 December 2020

Outcome of fetal cerebral posterior fossa anomalies

1 reference

12 December 2020

Hypoplastic left heart syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1002/PD.3943

1 reference

1 reference

1 reference

PubMed publication ID

22847778

1 reference