Always the most comprehensive resource, the MORL expands clinical MLPA, ADAMTS-13 and Classical Pathway Testing. Click here for details.
|OtoSCOPE provides comprehensive genetic testing for all genes implicated in non-syndromic hearing loss and many types of syndromic hearing loss. An Usher Syndrome Panel is also available.||The Genetic Renal Panel tests for genetic causes of TMA (aHUS and TTP) and C3G (DDD and C3GN). The Panel includes analysis for complex genomic rearrangements of the CFHR region.||Comprehensive complement testing includes quantitating complement proteins and their cleavage products, measuring complement activity, and screening for autoantibodies.|
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The University of Iowa
285 Newton Rd., 5270 CBRB
Iowa City, IA 52242
- Your results are discussed at a multidisciplinary meeting.
- Your testing is done in the Clinical Division of the MORL by scientists who lead the world in the human genetics of deafness and complement-mediated renal diseases.
- Your testing is the most comprehensive clinical testing available