Livia Marcato
Busto Arsizio, Italy
Last Updated: 09/26/2026
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Found 10 publications
First Trimester Screening for Common Trisomies and Microdeletion 22q11.2 Syndrome Using Cell-Free DNA: A Prospective Clinical Study.
Journal: Fetal diagnosis and therapy
Published: May 25, 2020
Implications of fetoplacental mosaicism on cell-free DNA testing for sex chromosome aneuploidies.
Journal: Prenatal diagnosis
Published: May 11, 2017
A pharmacogenetic-driven approach for controlled ovarian hyperstimulation by FSH treatment.
Journal: Minerva ginecologica
Published: November 06, 2014
Prenatal phenotype of Williams-Beuren syndrome and of the reciprocal duplication syndrome.
Journal: Clinical case reports
Published: September 10, 2013
De novo small supernumerary marker chromosomes detected on 143,000 consecutive prenatal diagnoses: chromosomal distribution, frequencies, and characterization combining molecular cytogenetics approaches.
Journal: Prenatal diagnosis
Published: June 24, 2013
QF-PCR as a substitute for karyotyping of cytotrophoblast for the analysis of chorionic villi: advantages and limitations from a cytogenetic retrospective audit of 44,727 first-trimester prenatal diagnoses.
Journal: Prenatal diagnosis
Published: April 23, 2013
Fetal mesenchymal stromal cells from cryopreserved human chorionic villi: cytogenetic and molecular analysis of genome stability in long-term cultures.
Journal: Cytotherapy
Published: December 19, 2012
Application of a new molecular technique for the genetic evaluation of products of conception.
Journal: Prenatal diagnosis
Published: November 22, 2012
Prenatal BACs-on-Beads™: the prospective experience of five prenatal diagnosis laboratories.
Journal: Prenatal diagnosis
Published: April 03, 2012
Showing 1-10 of 10
Last Updated: 09/26/2026