Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases-Reference-Cited by-同舟云学术

Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases

Published:2015-10-26 Issue:13 Volume:35 Page:1269-1277
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Papoulidis Ioannis¹,Sotiriadis Alexandros²,Siomou Elisavet¹,Papageorgiou Elena¹,Eleftheriades Makarios³,Papadopoulos Vasilios⁴,Oikonomidou Eirini⁵,Orru Sandro⁶,Manolakos Emmanouil¹,Athanasiadis Apostolos⁷

Affiliation:

1. Access To Genome - ATG P.C.; Thessaloniki Greece

2. Second Department of Obstetrics and Gynecology; Aristotle University of Thessaloniki; Thessaloniki Greece

3. EMBRYOCARE Fetal Medicine Center; Athens Greece

4. Department of Obstetrics and Gynecology; University of Patras Medical School; Patras Greece

5. EuroGenetica S.A.; Thessaloniki Greece

6. Department of Medical Genetics; Cagliari University, Binaghi Hospital; Cagliari Italy

7. First Department of Obstetrics and Gynecology; Aristotle University of Thessaloniki; Thessaloniki Greece

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Reference28 articles.

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2. Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies;Miller;Am J Hum Genet,2010

3. Prenatal diagnosis of chromosomal abnormalities using array-based comparative genomic hybridization;Sahoo;Genet Med,2006

4. Introducing array comparative genomic hybridization into routine prenatal diagnosis practice: a prospective study on over 1000 consecutive clinical cases;Fiorentino;Prenat Diagn,2011

5. Chromosomal microarray analysis as a first-line test in pregnancies with a priori low risk for the detection of submicroscopic chromosomal abnormalities;Fiorentino;Eur J Hum Genet,2013

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