Preimplantation genetic testing (PGT) for copy number variants of uncertain significance (CNV- VUS) in the genomic era: to do or not to do?
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R. Segel | G. Altarescu | S. Zeligson | T. Eldar‐Geva | O. Weiss | K. Rotshenker-Olshinka | Naama Srebnik Moshe | S. Shaviv | O. Freireich