A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings-Reference-Cited by-同舟云学术

A new direction for prenatal chromosome microarray testing: software-targeting for detection of clinically significant chromosome imbalance without equivocal findings

Published:2014-04-22 Issue: Volume:2 Page:e354
ISSN:2167-8359
Container-title:PeerJ
language:en
Short-container-title:

Author:

Ahn Joo Wook¹,Bint Susan²,Irving Melita D.³,Kyle Phillipa M.⁴,Akolekar Ranjit⁵,Mohammed Shehla N.³,Mackie Ogilvie Caroline¹⁶

Affiliation:

1. Cytogenetics, Guy’s & St Thomas’ NHS Foundation Trust, London, UK

2. Cytogenetics, GSTS Pathology, London, UK

3. Clinical Genetics, Guy’s & St Thomas’ NHS Foundation Trust, London, UK

4. Fetal Medicine Unit, Guy’s & St Thomas’ NHS Foundation Trust, London, UK

5. Fetal Medicine Unit, Medway Maritime Hospital, Kent, UK

6. King’s College, London, UK

Publisher

PeerJ

Subject

General Agricultural and Biological Sciences,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

Link

https://peerj.com/articles/354.pdf

Reference25 articles.

1. Array CGH as a first line diagnostic test in place of karyotyping for postnatal referrals—results from four years’ clinical application for over 8,700 patients;Ahn;Molecular Cytogenetics,2013

2. Validation and implementation of array comparative genomic hybridisation as a first line test in place of postnatal karyotyping for genome imbalance;Ahn;Molecular Cytogenetics,2010

3. An exploration of genetic counselors’ needs and experiences with prenatal chromosomal microarray testing;Bernhardt;Journal of Genetic Counseling,2014

4. Women’s experiences receiving abnormal prenatal chromosomal microarray testing results;Bernhardt;Genetics in Medicine,2013

5. A prospective study of the clinical utility of prenatal chromosomal microarray analysis in fetuses with ultrasound abnormalities and an exploration of a framework for reporting unclassified variants and risk factors;Brady;Genetics in Medicine,2013

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