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1. Pathogenic PHIP variants are variably associated with CAKUT

3. Letermovir Rescue Therapy in Kidney Transplant Recipients with Refractory/Resistant CMV Disease

8. Monoallelic intragenic POU3F2 variants lead to neurodevelopmental delay and hyperphagic obesity, confirming the gene’s candidacy in 6q16.1 deletions

9. Extended genomic HLA typing identifies previously unrecognized mismatches in living kidney transplantation

11. MO047: Biallelic pathogenic variants in ROBO1 associate with syndromic CAKUT

12. Biallelic pathogenic variants in roundabout guidance receptor 1 associate with syndromic congenital anomalies of the kidney and urinary tract

21. Matching clinical and genetic diagnoses in autosomal dominant polycystic kidney disease reveals novel phenocopies and potential candidate genes

27. Value of renal gene panel diagnostics in adults waiting for kidney transplantation due to undetermined end-stage renal disease

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