(Q27025214)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22887694%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

title

Microarray comparative genomic hybridization in prenatal diagnosis: a review (English)

1 reference

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11 February 2020

1

1 reference

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11 February 2020

Eamonn R Maher

4

1 reference

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11 February 2020

author name string

D J McMullan

2

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11 February 2020

D Williams

3

1 reference

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11 February 2020

M D Kilby

5

1 reference

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11 February 2020

language of work or name

1 reference

17 September 2012

1 reference

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Ultrasound in Obstetrics and Gynecology

11 February 2020

published in

2 references

PubMed

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22887694%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

volume

40

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PubMed

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11 February 2020

issue

4

2 references

PubMed

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11 February 2020

page(s)

385-391

1 reference

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Use of a DNA method, QF-PCR, in the prenatal diagnosis of fetal aneuploidies

11 February 2020

cites work

1 reference

Deletion of 150 kb in the minimal DiGeorge/velocardiofacial syndrome critical region in mouse.

21 January 2018

1 reference

Construction and use of spotted large-insert clone DNA microarrays for the detection of genomic copy number changes

21 January 2018

1 reference

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

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1 reference

Structural variation in the human genome

21 January 2018

1 reference

Global variation in copy number in the human genome

21 January 2018

1 reference

Integrated detection and population-genetic analysis of SNPs and copy number variation

21 January 2018

1 reference

Prenatal identification of a girl with a t(X;4)(p21;q35) translocation: molecular characterisation, paternal origin, and association with muscular dystrophy

21 January 2018

1 reference

Cryptic deletions are a common finding in "balanced" reciprocal and complex chromosome rearrangements: a study of 59 patients.

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities.

21 January 2018

1 reference

Mutations of the X-linked genes encoding neuroligins NLGN3 and NLGN4 are associated with autism

21 January 2018

1 reference

X-linked mental retardation and autism are associated with a mutation in the NLGN4 gene, a member of the neuroligin family

21 January 2018

1 reference

TBP as a candidate gene for mental retardation in patients with subtelomeric 6q deletions

21 January 2018

1 reference

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

21 January 2018

1 reference

Noninvasive prenatal diagnosis of fetal blood group phenotypes: current practice and future prospects

21 January 2018

1 reference

Non-invasive prenatal diagnosis of single gene disorders: how close are we?

21 January 2018

1 reference

Next-generation DNA sequencing techniques

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Presence of fetal DNA in maternal plasma and serum

21 January 2018

1 reference

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

21 January 2018

1 reference