Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Genes|December 23, 2022
Agnathia-Otocephaly Complex Due to a De Novo Deletion in the <i>OTX2</i> GeneMarco Fabiani, Francesco Libotte, Katia Margiotti, et al.
Journal of Prenatal Medicine|March 23, 2012
The use of DHPLC (Denaturing High Performance Liquid Chromatography) in II level screening of the CFTR gene in Prenatal DiagnosisAlvaro Mesoraca, Manuela Di Natale, Antonella Cima, et al.
Taiwanese Journal of Obstetrics & Gynecology|January 2, 2017
Pallister-Killian syndrome: Cytogenetics and molecular investigations of mosaic tetrasomy 12p in prenatal chorionic villus and in amniocytes. Strategy of prenatal diagnosisFrancesco Libotte, Domenico Bizzoco, Ivan Gabrielli, et al.
Prenatal Diagnosis|March 19, 2009
Antibiotic prophylaxis before second-trimester genetic amniocentesis (APGA): a single-centre open randomised controlled trialClaudio Giorlandino, Pietro Cignini, Marco Cini, et al.
Plos One|August 5, 2021
Multi-analytical test based on serum miRNAs and proteins quantification for ovarian cancer early detectionPriscila D R Cirillo, Katia Margiotti, Marco Fabiani, et al.
AJP Reports|May 25, 2013
Prenatal Diagnosis of a Fetus with de novo Supernumerary Ring Chromosome 16 Characterized by Array Comparative Genomic HybridizationPietro Cignini, Angela Dinatale, Laura D'Emidio, et al.
Molecular and Cellular Biochemistry|August 13, 2011
Metabolic profile of amniotic fluid as a biochemical tool to screen for inborn errors of metabolism and fetal anomaliesAngela M Amorini, Claudio Giorlandino, Salvatore Longo, et al.
Brain and Behavior|November 22, 2025
Maternal Folate Receptor Alpha Autoantibodies and Increased Fetal Nuchal Translucency as Potential Early Markers of Autism Spectrum DisorderClaudio Giorlandino, Katia Margiotti, Marco Fabiani, et al.
Journal of Prenatal Medicine|February 27, 2016
A new case of interstitial 1q 25.3-32.1 deletion: cytogenetic analysis molecular characterization and ultrasound findingsFrancesco Libotte, Domenico Bizzoco, Ivan Gabrielli, et al.
Journal of Assisted Reproduction and Genetics|December 18, 2024
Uniparental disomy (UPD) exclusion in embryos following Preimplantation Genetic Testing for Structural Rearrangements (PGT-SR)Marco Fabiani, Katia Margiotti, Francesco Libotte, et al.
Pageof 5