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Issue DateTitleAuthor(s)
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.
3 September 2016Beta cell function and ongoing autoimmunity in long-standing, childhood onset type 1 diabetes. Williams, GM; Long, AE; Wilson, IV; et al.
31 March 2016Successful transfer to sulfonylureas in KCNJ11 neonatal diabetes is determined by the mutation and duration of diabetes Babiker, T; Vedovato, N; Patel, K; et al.
28 April 2016Practical Classification Guidelines for Diabetes in patients treated with insulin: a cross-sectional study of the accuracy of diabetes diagnosis. Hope, SV; Wienand-Barnett, S; Shepherd, M; et al.
1 September 2016Prematurity should not prevent genetic testing for neonatal diabetes Besser, RE; Flanagan, SE; Mackay, DG; et al.
1 October 2016Monogenic autoimmune diseases of the endocrine system Johnson, MB; Hattersley, AT; Flanagan, SE
28 September 2016Genome-wide associations for birth weight and correlations with adult disease Horikoshi, M; Beaumont, RN; Day, FR; et al.
8 April 2016Differential regulation of serum microRNA expression by HNF1β and HNF1α transcription factors. Fendler, W; Madzio, J; Kozinski, K; et al.
27 April 2016Neonatal diabetes caused by a homozygous KCNJ11 mutation demonstrates that tiny changes in ATP sensitivity markedly affect diabetes risk. Vedovato, N; Cliff, E; Proks, P; et al.
17 August 2016Hypogonadotropic hypogonadism and short stature in patients with diabetes due to neurogenin 3 deficiency Rubio-Cabezas, O; Luis Gómez, J; Gleisner, A; et al.
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    Hattersley, AT20
  • Ellard, S10
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    201620
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