Cargando…
Non-invasive prenatal screening: A 20-year experience in Italy
Over the past two decades, there has been a rapid evolution in prenatal screening for fetal chromosome abnormalities. Initially, testing was focused on the identification of affected pregnancies in either the first, or, the second trimester (e.g. the Combined test or the triple test). This was repla...
Autores principales: | Palka, Chiara, Guanciali-Franchi, Paolo, Morizio, Elisena, Alfonsi, Melissa, Papponetti, Marco, Sabbatinelli, Giulia, Palka, Giandomenico, Calabrese, Giuseppe, Benn, Peter |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6687402/ https://www.ncbi.nlm.nih.gov/pubmed/31403132 http://dx.doi.org/10.1016/j.eurox.2019.100050 |
Ejemplares similares
-
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis
por: Guanciali Franchi, Paolo, et al.
Publicado: (2017) -
Aneuploidy screening using circulating fetal cells in maternal blood by dual‐probe FISH protocol: a prospective feasibility study on a series of 172 pregnant women
por: Calabrese, Giuseppe, et al.
Publicado: (2016) -
Isolation and Enrichment of Circulating Fetal Cells for NIPD: An Overview
por: Sabbatinelli, Giulia, et al.
Publicado: (2021) -
First case of two supernumerary markers derived from chromosome 5 and chromosome 8
por: Giansante, Roberta, et al.
Publicado: (2022) -
Mayer-Rokitansky-Küster-Hauser syndrome with 22q11.21 microduplication: a case report
por: Dell’Edera, Domenico, et al.
Publicado: (2021)