MORL: A Clinical Revolution - At the Forefront of Precision Medicine for Hearing Impairment (video)
MORL: The Cutting Edge of Research - Revolutionizing Genetic Research for Hearing Loss (video)
Always the most comprehensive resource, the MORL expands clinical MLPA, ADAMTS-13 and Classical Pathway Testing. Click 
here for details.
Featured Content
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Genetic Hearing Loss |
Genetic Renal Panel |
Complement Tests |
| 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. |
Helping to Make Lives Better (Videos)
The University of Iowa
285 Newton Rd., 5270 CBRB
Iowa City, IA 52242
Phone: 319-335-6623
Fax: 319-353-5869
Email: morl@uiowa.edu
What does it mean to get your testing done at the MORL?
- 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