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shirinnyy shirinnyy
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Posts: 1004
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6 years ago
The nurse in the genetics clinic is working with families undergoing testing for genetic disease. If the initial testing is positive, more extensive testing is required to confirm:
 
  1. Pre-implantation genetic diagnosis.
 
  2. Prenatal diagnostic testing.
 
  3. Newborn screening.
 
  4. Carrier screening.
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wrote...
6 years ago
3, newborn screening.

Rationale:

1. Results from pre-implantation genetic diagnosis, prenatal diagnostic testing, and carrier screening have higher levels of specificity and sensitivity.
2. Results from pre-implantation genetic diagnosis, prenatal diagnostic testing, and carrier screening have higher levels of specificity and sensitivity.
3. Newborn screening for phenylketonuria, or sickle-cell or maple syrup urine disease, when positive, must be confirmed with more extensive testing.
4. Results from pre-implantation genetic diagnosis, prenatal diagnostic testing, and carrier screening have higher levels of specificity and sensitivity.
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