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Helping to Make Lives Better (Videos)
The University of Iowa5270 CBRB | Iowa City, IA 52242Phone: 319-335-6623 Fax: 319-353-5869Email: email@example.com
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OtoSCOPE provides comprehensive genetic testing for all genes implicated in non-syndromic hearing loss, Usher syndrome, and Pendred syndrome. An Usher Syndrome Panel is also available.
The Genetic Renal Panel attempts to determine the genetic cause of patients diagnosed with TMAs; in the past this required multiple tests, the Genetic Renal Panel accomplishes the same objectives with one.
The MORL offers unique and specific assays for several complement-mediated diseases (C3GN, DDD, aHUS) to define complement profiles as an aid to patient care.