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Precision Medicine
FRAGILE X IN WHOLE BLOOD
What you need to know about study FRAGILE X IN WHOLE BLOOD
What is this study and what is it for?
Confirmation of Fragile X syndrome, Fragile X tremor/ataxia syndrome, or premature ovarian failure diagnosis caused by FMR1 gene expansions. Carrier status determination for people with a family history of Fragile X syndrome or X-linked intellectual disability. Prenatal diagnosis of fragile X syndrome when there is a documented expansion of FMR1 in the family.
What type of sample is needed?
Whole blood
Preparation / Instructions
All prenatal samples must be accompanied by a maternal blood sample
Delivery time
14 business days
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The information published on this site is for informational and educational purposes. It is not a substitute for medical consultation, professional diagnosis, or treatment prescribed by a specialist. If you have any questions regarding symptoms, test results, or laboratory studies, please consult your doctor.