Browsing by Author "Clissold, RL"
Now showing items 1-5 of 5
Issue Date | Title | Author(s) |
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22 May 2015 | Assessment of the HNF1B Score as a Tool to Select Patients for HNF1B Genetic Testing | Clissold, RL; Shields, B; Ellard, Sian; et al. |
24 May 2016 | Chromosome 17q12 microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorder. | Clissold, RL; Shaw-Smith, C; Turnpenny, P; et al. |
30 January 2018 | Exocrine pancreatic dysfunction is common in hepatocyte nuclear factor 1β-associated renal disease and can be symptomatic | Clissold, RL; Fulford, J; Hudson, M; et al. |
18 July 2018 | Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion. | Clissold, RL; Ashfield, B; Burrage, J; et al. |
1 February 2015 | HNF1B-associated renal and extra-renal disease-an expanding clinical spectrum. | Clissold, RL; Hamilton, Alexander; Hattersley, Andrew T.; et al. |