WebJul 18, 2024 · Heterozygous mutation of the transcription factor HNF1B is the most common cause of monogenetic developmental renal disease. Disease-associated mutations fall … WebBibTeX @MISC{Edghill_originalarticle, author = {Emma L. Edghill and Richard A. Oram and Martina Owens and Karen L. Stals and Lorna W. Harries and Andrew T. Hattersley and Sian Ellard and Coralie Bingham}, title = {Original Article}, year = {}}

CiteSeerX — Original Article - Pennsylvania State University

WebRenal cysts are the most frequently detected feature of HNF1B-associated kidney disease; however, other structural abnormalities, including single kidneys and renal hypoplasia, … WebPublications by authors named "Coralie Bingham" 9,999,999 Publications. Page 1 of 1 core isolation memory integration

CiteSeerX — Original Article - Pennsylvania State University

WebBibTeX @MISC{Edghill_originalarticle, author = {Emma L. Edghill and Richard A. Oram and Martina Owens and Karen L. Stals and Lorna W. Harries and Andrew T. Hattersley … WebOct 1, 2010 · Semantic Scholar extracted view of "Mutations in the hepatocyte nuclear factor-1β (HNF1B) gene are common with combined uterine and renal malformations but are not found with isolated uterine malformations." by R. Oram et al. WebCoralie Bingham. Honorary Associate Professor, Consultant in Renal Medicine, Exeter Kidney Unit. [email protected] / [email protected]. +44 (0) 1392 40 6366. … fancit helpdesk