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Alvaro Mesoraca

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Journal of Prenatal Medicine|October 22, 2014
Six consecutive false positive cases from cell-free fetal DNA testing in a single referring centreNella Dugo, Francesco Padula, Luisa Mobili, et al.
BMC Research Notes|March 20, 2020
Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experienceKatia Margiotti, Anthony Cesta, Claudio Dello Russo, et al.
The Journal of Molecular Diagnostics : JMD|April 28, 2019
Validation of Extensive Next-Generation Sequencing Method for Monogenic Disorder Analysis on Cell-Free Fetal DNA: Noninvasive Prenatal DiagnosisClaudio Dello Russo, Anthony Cesta, Salvatore Longo, et al.
Journal of Medicine and Life|January 18, 2021
Cytogenetics and Molecular Investigations detect a Mosaic Variant of Turner Syndrome only Suspected by Non-Invasive Prenatal Testing: Two Case Reports with Negative Ultrasound ExaminationsFrancesco Libotte, Sonia Lorena Carpineto, Claudio Dello Russo, et al.
Journal of Prenatal Medicine|March 23, 2012
Proteomic analysis for the study of amniotic fluid protein compositionMarzia Perluigi, Fabio Di Domenico, Chiara Cini, et al.
Methods and Protocols|June 25, 2026
Folate Receptor Alpha Autoantibodies in Early Pregnancy: First-Trimester Reference Intervals and Proposed Clinical ThresholdsClaudio Giorlandino, Marina Cupellaro, Katia Margiotti, et al.
Genetics Research|June 17, 2020
Cell-free DNA screening for aneuploidies in 7113 pregnancies: single Italian centre studyAlvaro Mesoraca, Katia Margiotti, Claudio Dello Russo, et al.
Diagnostics (Basel, Switzerland)|November 27, 2024
Compound Heterozygous Variants in the <i>IFT140</i> Gene Associated with Skeletal CiliopathiesKatia Margiotti, Marco Fabiani, Antonella Cima, et al.
Neurogenetics|August 15, 2025
Pathogenic KCNH2 variant in monozygotic twins with speech delay and lower risk type 2 long QT syndromeKatia Margiotti, Marco Fabiani, Costanza Zangheri, et al.
Journal of Prenatal Medicine|August 13, 2015
Comparative study of aCGH and Next Generation Sequencing (NGS) for chromosomal microdeletion and microduplication screeningClaudio Dello Russo, Gianluca Di Giacomo, Pietro Cignini, et al.
Pageof 5

Showing results (21-30 of 43) with videos related to

Sort By:
Pageof 5
Journal of Prenatal Medicine|October 22, 2014
Six consecutive false positive cases from cell-free fetal DNA testing in a single referring centreNella Dugo, Francesco Padula, Luisa Mobili, et al.
BMC Research Notes|March 20, 2020
Cell-free DNA screening for sex chromosomal aneuploidies in 9985 pregnancies: Italian single experienceKatia Margiotti, Anthony Cesta, Claudio Dello Russo, et al.
The Journal of Molecular Diagnostics : JMD|April 28, 2019
Validation of Extensive Next-Generation Sequencing Method for Monogenic Disorder Analysis on Cell-Free Fetal DNA: Noninvasive Prenatal DiagnosisClaudio Dello Russo, Anthony Cesta, Salvatore Longo, et al.
Journal of Medicine and Life|January 18, 2021
Cytogenetics and Molecular Investigations detect a Mosaic Variant of Turner Syndrome only Suspected by Non-Invasive Prenatal Testing: Two Case Reports with Negative Ultrasound ExaminationsFrancesco Libotte, Sonia Lorena Carpineto, Claudio Dello Russo, et al.
Journal of Prenatal Medicine|March 23, 2012
Proteomic analysis for the study of amniotic fluid protein compositionMarzia Perluigi, Fabio Di Domenico, Chiara Cini, et al.
Methods and Protocols|June 25, 2026
Folate Receptor Alpha Autoantibodies in Early Pregnancy: First-Trimester Reference Intervals and Proposed Clinical ThresholdsClaudio Giorlandino, Marina Cupellaro, Katia Margiotti, et al.
Genetics Research|June 17, 2020
Cell-free DNA screening for aneuploidies in 7113 pregnancies: single Italian centre studyAlvaro Mesoraca, Katia Margiotti, Claudio Dello Russo, et al.
Diagnostics (Basel, Switzerland)|November 27, 2024
Compound Heterozygous Variants in the <i>IFT140</i> Gene Associated with Skeletal CiliopathiesKatia Margiotti, Marco Fabiani, Antonella Cima, et al.
Neurogenetics|August 15, 2025
Pathogenic KCNH2 variant in monozygotic twins with speech delay and lower risk type 2 long QT syndromeKatia Margiotti, Marco Fabiani, Costanza Zangheri, et al.
Journal of Prenatal Medicine|August 13, 2015
Comparative study of aCGH and Next Generation Sequencing (NGS) for chromosomal microdeletion and microduplication screeningClaudio Dello Russo, Gianluca Di Giacomo, Pietro Cignini, et al.
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