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Prenatal genetic testing to identify hereditary conditions
For expectant parents, who value their baby’s well-being above all else, prenatal testing can provide critical insights on their child’s health. Our full menu of clinically supported prenatal testing enables results that patients and physicians can depend on.
Featuring carrier screening options and diagnostic testing, our offerings include testing for a variety of genetic conditions, including known familial variants. We also offer cytogenetic analysis options such as karyotype, targeted fluorescent in situ hybridization (FISH), and microarray to evaluate for chromosomal aneuploidy and microdeletion/microduplication syndromes.
Commitment to care
At Mayo Clinic Laboratories, our meticulous care of prenatal samples throughout all laboratory processes ensures all appropriate testing can be completed. From careful handling of specimens upon receipt to expeditious reporting of clinically relevant results, we are dedicated to providing unmatched service to physicians and their patients. Key benefits of our testing include:
Beyond the test result
When you partner with Mayo Clinic Laboratories, you gain access to leading experts in the field of prenatal diagnostics. Our prenatal testing laboratories are staffed by dedicated teams of laboratory directors, genetic counselors, and scientists working in a state-of-the-art environment. This team provides testing and result interpretation of the highest quality for the diagnosis and clinical care of prenatal disorders.