Preimplantation genetic testing (PGT) for copy number variants of uncertain significance (CNV- VUS) in the genomic era: to do or not to do?

PURPOSE: To review cases of couples presented to our PGT-unit with copy number variants (CNVs) classified as variants of uncertain significance (VUS) in order to better understand their needs. METHODS: Retrospective cohort study conducted in a tertiary medical-center, 2014–2019. We reviewed files of...

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Detalhes bibliográficos
Publicado no:J Assist Reprod Genet
Main Authors: Rotshenker-Olshinka, Keren, Srebnik Moshe, Naama, Weiss, Omri, Shaviv, Shira, Freireich, Orit, Segel, Reeval, Zeligson, Sharon, Eldar-Geva, Talia, Altarescu, Gheona
Formato: Artigo
Idioma:Inglês
Publicado em: Springer US 2021
Assuntos:
Genetics
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7910379/
https://ncbi.nlm.nih.gov/pubmed/33443723
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1007/s10815-020-02055-3
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