Detecting fetal subchromosomal aberrations by MPS: an unexpected discrepancy between amniocyte DNA and ccffDNA-Reference-Cited by-同舟云学术

Detecting fetal subchromosomal aberrations by MPS: an unexpected discrepancy between amniocyte DNA and ccffDNA

Published:2014-02-06 Issue:4 Volume:34 Page:402-405
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Buysse Karen¹,de Ligt Joep¹,Janssen Irene M.¹,van Bon Bregje W. M.¹,Gomes Ingrid¹,Hehir-Kwa Jayne¹,Eggink Alex J.²,van Vugt John M. G.³,Vissers Lisenka E. L. M.¹,Geurts van Kessel Ad¹,Faas Brigitte H. W.¹

Affiliation:

1. Department of Human Genetics; Radboud University Medical Center; Nijmegen the Netherlands

2. Department of Obstetrics and Gynaecology, Erasmus MC; University Medical Center; Rotterdam the Netherlands

3. Department of Obstetrics and Gynaecology; Radboud University Medical Center; Nijmegen the Netherlands

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference12 articles.

1. Presence of fetal DNA in maternal plasma and serum;Lo;Lancet,1997

2. Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma;Chiu;Proc Natl Acad Sci USA,2008

3. Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood;Fan;Proc Natl Acad Sci USA,2008

4. Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasma;Srinivasan;Am J Hum Genet,2013

5. Optimal detection of fetal chromosomal abnormalities by massively parallel DNA sequencing of cell-free fetal DNA from maternal blood;Sehnert;Clin Chem,2011

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2. Implementation of whole genome massively parallel sequencing for noninvasive prenatal testing in laboratories;Expert Review of Molecular Diagnostics;2014-10-27