학술논문
Positive Predictive Values and Outcomes for Uninformative Cell-Free DNA Tests: An Italian Multicentric Cytogenetic and Cytogenomic Audit of DiagnOstic Testing (ICARO Study)
Document Type
Article
Author
Grati, Francesca Romana; Bestetti, Ilaria; de Siero, Daria; Malvestiti, Francesca; Villa, Nicoletta; Sala, Elena; Crosti, Francesca; Parisi, Valentina; Nardone, Anna Maria; Di Giacomo, Gianluca; Pettinari, Antonella; Tortora, Giada; Montaldi, Annamaria; Calò, Annapaola; Saccilotto, Donatella; Zanchetti, Sara; Celli, Paola; Guerneri, Silvana; Silipigni, Rosamaria; Cardarelli, Laura; Lippi, Elisabetta; Cavani, Simona; Malacarne, Michela; Genesio, Rita; Beltrami, Nicola; Pittalis, Maria Carla; Desiderio, Laura; Gentile, Mattia; Ficarella, Romina; Recalcati, Maria Paola; Catusi, Ilaria; Garzo, Maria; Miele, Lorena; Corti, Cecilia; Ghezzo, Sara; Bertini, Veronica; Cambi, Francesca; Valetto, Angelo; Facchinetti, Barbara; Bernardini, Laura; Capalbo, Anna; Balducci, Federica; Pelo, Elisabetta; Minuti, Barbara; Pescucci, Chiara; Giuliani, Costanza; Renieri, Alessandra; Longo, Ilaria; Tita, Rossella; Castello, Giuseppe; Casalone, Rosario; Righi, Rossana; Raso, Barbara; Civolani, Alessandro; Muzi, Maria Cristina; di Natale, Manuela; Varriale, Luigia; Gasperini, Daniela; Nuzzi, Maria Cristina; Cellamare, Angelo; Casieri, Paola; Busuito, Rosa; Ceccarini, Caterina; Cesarano, Carla; Privitera, Orsola; Melani, Daniela; Menozzi, Cristina; Falcinelli, Cristina; Calabrese, Olga; Battaglia, Paola; Tanzariello, Antonella; Stampalija, Tamara; Ardisia, Carmela; Gasparini, Paolo; Benn, Peter; Novelli, Antonio
Source
Obstetrical and Gynecological Survey; June 2023, Vol. 78 Issue: 6 p318-320, 3p
Subject
Language
ISSN
00297828; 15339866
Abstract
(Abstracted from Prenat Diagn2022;42:1575–1586Methods for diagnosis of genetic abnormalities have recently undergone substantial improvement. Noninvasive prenatal testing (NIPT) is performed early in pregnancy, typically at the end of the first trimester using cell-free DNA (cfDNA) to identify 3 commonly occurring trisomies (13, 18, and 21).