Now showing items 1-5 of 5

    Issue DateTitleAuthor(s)
    22 May 2015Assessment of the HNF1B Score as a Tool to Select Patients for HNF1B Genetic Testing  Clissold, RL; Shields, B; Ellard, Sian; et al.
    24 May 2016Chromosome 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 2018Exocrine 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 2018Genome-wide methylomic analysis in individuals with HNF1B intragenic mutation and 17q12 microdeletion.  Clissold, RL; Ashfield, B; Burrage, J; et al.
    1 February 2015HNF1B-associated renal and extra-renal disease-an expanding clinical spectrum.  Clissold, RL; Hamilton, Alexander; Hattersley, Andrew T.; et al.