Fingerprint
Dive into the research topics of 'HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort'. Together they form a unique fingerprint.- Sort by
- Weight
- Alphabetically
HNF1B and PAX2 mutations are a common cause of renal hypodysplasia in the CKiD cohort
Rosemary Thomas, Simone Sanna-Cherchi, Bradley A. Warady, Susan L. Furth, Frederick J. Kaskel, Ali G. Gharavi
Research output: Contribution to journal › Article › peer-review
102
Scopus
citations