Results 141 to 150 of about 5,809 (168)

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

Prenatal Diagnosis, 2012
ABSTRACTObjectiveEvaluate the results obtained from Quantitative Fluorescent (QF)‐PCR and conventional karyotype analysis to determine the advantages and disadvantages of dual testing in prenatal diagnosis.MethodsFrom 1 June 2006 to 1 June 2010, dual testing by QF‐PCR and karyotype analysis was performed in 13 500 prenatal samples.
Ioannis, Papoulidis, Elisavet, Siomou, Alexandros, Sotiriadis, George, Efstathiou, Anastasia, Psara, Eirini, Sevastopoulou, Eleftherios, Anastasakis, Stavros, Sifakis, Theodora, Tsiligianni, Maria, Kontodiou, Christine, Malamaki, Maria, Tzimina, Michael Bjorn, Petersen, Emmanouil, Manolakos, Apostolos, Athanasiadis   +14 more
openaire   +2 more sources

Huntington disease–unaffected fetus diagnosed from maternal plasma using QF‐PCR

Prenatal Diagnosis, 2003
AbstractThe discovery of fetal DNA in maternal plasma from early pregnancies has led to new opportunities for clinical application. In the last few years there have been numerous reported applications, mainly fetal gender and RhD genotyping. The prenatal diagnosis of some inherited genetic diseases such as Huntington disease is also very frequently ...
M C, González-González, M J, Trujillo, M, Rodríguez de Alba, M, García-Hoyos, I, Lorda-Sánchez, J, Díaz-Recasens, C, Ayuso, C, Ramos   +7 more
openaire   +2 more sources

Prenatal detection of chromosome disorders by QF-PCR

The Lancet, 2001
M, Adinolfi, J, Sherlock
openaire   +2 more sources

[Rapid prenatal diagnosis of chromosome abnormalities: from FISH to QF-PCR].

Revue medicale suisse, 2005
Prenatal diagnosis for pregnancies at increased risk for chromosome abnormalities is routinely undertaken by karyotype analysis. While karyotype analysis remains the standard method to detect structural and copy number changes of chromosomes, it requires prolonged cell culture resulting in average reporting times of about two weeks. To relieve parental
Bernard, Conrad, Frédérique, Bena, Sophie, Dahoun-Hadorn   +2 more
openaire   +1 more source

PCR Past, Present and Future

BioTechniques, 2020
Hanliang Zhu, Haoqing Zhang, Marie Korabečná   +2 more
exaly  

PGD by aCGH and QF-PCR in a couple with recurring aneuploidies

JBRA Assisted Reproduction, 2012
Andressa G Mondadori, Maria Eugenia Ducatelli, Judith Mincman, Alicia Gallo, Fabián Coco, Roberto Coco   +5 more
openaire   +1 more source

Fetal Anöploidi Açısından Yüksek Riskli Gebeliklerin QF-PCR İle Analizi

2013
Kantitatif fluoresan polimeraz zincir reaksiyon (Quantitative Fluorescent Polymerase Chain Reaction, QF-PCR) yöntemi yaygın kromozom anormalliklerine yönelik yapılan düşük maliyetli, hızlı ve otomasyon sağlayan avantajlı bir prenatal tanı yöntemidir. Hastanemizde prenatal anöploidi taramasında aktif olarak kullanılmaktadır.
GÜNGÖR, Ayşe Nur Çakır, HACIVELİOĞLU, Servet, ULUDAĞ, Ahmet, GENCER, Meryem, UYSAL, Ahmet, ATİK, Sinem, COŞAR, Emine, SILAN, Fatma, ÖZDEMİR, Öztürk   +8 more
openaire   +4 more sources

Rapid PCR powered by microfluidics: A quick review under the background of COVID-19 pandemic

TrAC - Trends in Analytical Chemistry, 2021
Xiaobin Dong, Lulu Zhang, Shengxiang Ge   +2 more
exaly  

PCR enhancers: Types, mechanisms, and applications in long-range PCR

Biochimie, 2022
Martin A Kennedy, Eng Wee Chua
exaly  

Identifying CUP tumours with PCR

Nature Reviews Clinical Oncology, 2012
Mina Razzak, Razzak Mina
exaly