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Now showing items 11-20 of 87

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Issue DateTitleAuthor(s)
2 April 2014GATA4 mutations are a cause of neonatal and childhood-onset diabetes Shaw-Smith, C; De Franco, E; Lango Allen, H; et al.
10 August 2015Expanding the Clinical Spectrum Associated With GLIS3 Mutations Dimitri, P; Habeb, AM; Garbuz, F; et al.
2014Identifying good responders to glucose lowering therapy in type 2 diabetes: implications for stratified medicine Jones, AG; Shields, BM; Hyde, CJ; et al.
28 December 2012Identifying clinical criteria to predict Type 1 diabetes, as defined by absolute insulin deficiency: a systematic review protocol. Shields, BM; Peters, JL; Cooper, C; 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, AT73
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