Dual testing with QF-PCR and karyotype analysis for prenatal diagnosis of chromosomal abnormalities. Evaluation of 13 500 cases with consideration of using QF-PCR as a stand-alone test according to referral indications-Reference-Cited by-同舟云学术

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Dual testing with QF-PCR and karyotype analysis for prenatal diagnosis of chromosomal abnormalities. Evaluation of 13 500 cases with consideration of using QF-PCR as a stand-alone test according to referral indications

Published:2012-04-18 Issue:7 Volume:32 Page:680-685
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat Diagn

Author:

Papoulidis Ioannis¹,Siomou Elisavet¹,Sotiriadis Alexandros²,Efstathiou George¹,Psara Anastasia³,Sevastopoulou Eirini³,Anastasakis Eleftherios⁴,Sifakis Stavros⁵,Tsiligianni Theodora¹,Kontodiou Maria¹,Malamaki Christine¹,Tzimina Maria¹,Petersen Michael Bjorn¹,Manolakos Emmanouil¹,Athanasiadis Apostolos²

Affiliation:

1. Eurogenetica SA; Athens Thessaloniki Greece

2. School of Medicine; Aristotle University of Thessaloniki; Thessaloniki Greece

3. Centre of Fetal Medicine; Thessaloniki Greece

4. Athens Navy Hospital; Athens Greece

5. Department of Obstetrics and Gynecology; University of Crete; Heraklion Greece

Publisher

Wiley

Subject

Genetics(clinical),Obstetrics and Gynaecology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/pd.3888/fullpdf

Reference20 articles.

1. Diagnosis of Down syndrome and other aneuploidies using quantitative polymerase chain reaction and small tandem polymorphisms;Mansfield;Hum Mol Genet,1993

2. Rapid molecular method for prenatal detection of Down's syndrome;Pertl;Lancet,1994

3. Rapid and simple prenatal DNA diagnosis of Down's syndrome;Verma;Lancet,1998

4. Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, 21 by FISH or PCR without a full karyotype: a cytogenetic risk assessment;Caine;Lancet,2005

5. Evaluation of molecular tests for prenatal diagnosis of chromosome abnormalities;Grimshaw;Health Technol Assess,2003

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1. The Effect of Resolution Level and Targeted Design in the Diagnostic Performance of Prenatal Chromosomal Microarray Analysis;Fetal Diagnosis and Therapy;2023

2. Contribution of maternal mosaicism to false-positive chromosome X loss associated with noninvasive prenatal testing;The Journal of Maternal-Fetal & Neonatal Medicine;2022-03-13

3. Clinical Selection of Prenatal Diagnostic Techniques Following Positive Noninvasive Prenatal Screening Results in Southwest China;Frontiers in Genetics;2022-01-28

4. The Relationship between Prenatal Diagnosis Indications and Abnormal Chromosomal Karyotypes: A Retrospective Cohort of 4646 Cases in Beijing from 2012-2019;Current Topics in Medicinal Chemistry;2021-05

5. Comparison of quantitative fluorescent polymerase chain reaction and karyotype analysis for prenatal screening of chromosomal aneuploidies in 270 amniotic fluid samples;Journal of Perinatal Medicine;2019-08-27

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