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The American Journal of Pathology|November 14, 2000
Potential biological role of transforming growth factor-beta1 in human congenital kidney malformationsS P Yang, A S Woolf, H T Yuan, et al.
Journal of Nephrology|June 5, 2024
A targeted gene panel illuminates pathogenesis in young people with unexplained kidney failureFelicity Beal, Natalie Forrester, Elizabeth Watson, et al.
Pediatric Nephrology (Berlin, Germany)|May 10, 2011
Renal FMD may not confer a familial hypertensive risk nor is it caused by ACTA2 mutationsStephen D Marks, Ambrose M Gullett, Eileen Brennan, et al.
Prenatal Diagnosis|December 6, 2023
When should we offer antenatal sequencing for urinary tract malformations? A systematic review, cohort study and meta-analysisSarah Sonner, Kelly Reilly, Adrian S Woolf, et al.
American Journal of Medical Genetics. Part A|January 11, 2019
22q11.2 duplications in a UK cohort with bladder exstrophy-epispadias complexGlenda M Beaman, Adrian S Woolf, Raimondo M Cervellione, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|September 12, 2009
Analysis of TSHZ2 and TSHZ3 genes in congenital pelvi-ureteric junction obstructionDagan Jenkins, Xavier Caubit, Aleksandar Dimovski, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|June 8, 2001
Multicystic dysplastic kidney and Kallmann's syndrome: a new association?A Deeb, A Robertson, G MacColl, et al.
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