Dear Colleagues,   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! |   |
Disease |
Genes |
Paperwork/Unterlagen |
Urinary Tract Malformations CAKUT |
ACE
AGT AGTR1 BMP4 EYA1 GATA3 HNF1B KAL1 PAX2 REN RET ROBO2 SALL1 SIX1 SIX2 SIX5 SOX17 TNXB UPK3A WNT4 |
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