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Precision Medicine
CYSTIC FIBROSIS MUTATION
What you need to know about study CYSTIC FIBROSIS MUTATION
What is this study and what is it for?
Confirmation of cystic fibrosis clinical diagnosis. Risk refinement through carrier screening for individuals in the general population. Prenatal diagnosis or familial variant testing when familial variants are included in the 106-variant panel listed in Clinical Information. Risk refinement through carrier screening for people with a family history when family mutations are not available. Identification of patients who may respond to therapy with CFTR enhancers.
What type of sample is needed?
Whole blood
Preparation / Instructions
No special indications
Delivery time
10 business days
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