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- W3145667584 abstract "Abstract Preimplantation genetic testing for monogenic diseases (PGT-M) was introduced in assisted reproductive programs as a preventive test for patients identified as having high risk for inherited Mendelian conditions. PGT-M is considered an early prenatal diagnosis for monogenic conditions with the advantage of avoiding or limiting the decisions of termination of pregnancy as only genetically normal embryos are transferred to the uterus. In recent years, the implementation of new methods and improvements to in vitro fertilization programs, such as vitrification and trophectoderm biopsy, has enabled the achievement of better clinical results after embryo testing. In parallel, advancements in genetic knowledge, technology, and molecular methods have allowed for the possibility of offering an ever-expanded list of conditions to be tested in embryo biopsies. In this chapter, this evolution is described and current PGT strategies where testing for monogenic and aneuploidy screening preimplantation genetic testing for aneuploidies from the same embryo sample is the standard for all PGT-M indications are explained." @default.
- W3145667584 created "2021-04-13" @default.
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- W3145667584 date "2020-01-01" @default.
- W3145667584 modified "2023-09-25" @default.
- W3145667584 title "Preimplantation genetic testing for monogenic diseases" @default.
- W3145667584 doi "https://doi.org/10.1016/b978-0-12-816561-4.00015-6" @default.
- W3145667584 hasPublicationYear "2020" @default.
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