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Molecular Genetics and Metabolism Reports|September 4, 2023
The role of genetic testing in suspected fulminant myocarditis: A case reportRaffaella Mistrulli, Caterina Micolonghi, Federico Follesa, et al.
Current Issues in Molecular Biology|March 28, 2023
A Novel Nonsense Pathogenic <i>TTN</i> Variant Identified in a Patient with Severe Dilated CardiomyopathyCaterina Micolonghi, Marco Fabiani, Erika Pagannone, et al.
Human Reproduction (Oxford, England)|March 17, 2023
The use of copy number loads to designate mosaicism in blastocyst stage PGT-A cycles: fewer is betterLaura Girardi, Matteo Figliuzzi, Maurizio Poli, et al.
Reproductive Biomedicine Online|July 7, 2022
Maternal exome analysis for the diagnosis of oocyte maturation defects and early embryonic developmental arrestAntonio Capalbo, Silvia Buonaiuto, Matteo Figliuzzi, et al.
American Journal of Human Genetics|March 30, 2020
Incidence, Origin, and Predictive Model for the Detection and Clinical Management of Segmental Aneuploidies in Human EmbryosLaura Girardi, Munevver Serdarogullari, Cristina Patassini, et al.
Fertility and Sterility|June 7, 2026
Cost effectiveness of routine utilisation of atypically-pronucleated zygotes in IVF cycles with preimplantation genetic testingAntonio Capalbo, Francesca Mulas, Rebecca Cavagnola, et al.
European Journal of Human Genetics : EJHG|May 31, 2025
MYBPC3 c.2309-2A>G: exploring a founder variant in Italian hypertrophic cardiomyopathy patientsMarco Fabiani, Caterina Micolonghi, Silvia Caroselli, et al.
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