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A couple, both carriers of cystic fibrosis (CF) alleles, can decrease their odds of having a child with CF by performing an in vitro fertilization procedure and screening the embryo for the CF alleles. This process is called

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The procedure can decrease the odds of having a child with CF by performing an in vitro fertilization procedure and screening the embryo for the CF alleles is referred to as preimplantation genetic diagnosis.

What diseases can be detected by preimplantation genetic diagnosis?

Pre-implantation genetic diagnosis (PGD) is the testing of embryos or oocytes at the pre-implantation stage for genetic defects.

It can be used to diagnose cystic fibrosis, Tay-Sachs disease, Hemophilia, etc.

Thus, the procedure can decrease the odds of having a child with CF by performing an in vitro fertilization procedure and screening the embryo for the CF alleles is referred to as preimplantation genetic diagnosis.

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