We are happy to include your patient in our mutation analysis in single-gene causes of urinary tract malformations/congenital abnormalities of the kidney and urinary tract (CAKUT).
Please inform the patient/parents that this process may take more than 6 months. If you do not hear from us that means we have not found the disease-causing mutation. In case we find the disease-causing mutation we may help you initiate CLIA-certified mutation analysis.
We will provide free shipment for the blood samples. To get started, please follow the instructions below.
Thank you for your interest!
Urinary Tract Malformations
I have not completed CITI-Training: "How-to manual - PDF document"
I have completed CITI-Training: Please contact Dr. Nina Mann
If you are an enrolled collaborator, please click here
If you are an enrolled collaborator and the participant is a non-English speaker, please click here
Last update on May, 2019