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Now showing items 21-30 of 87

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Issue DateTitleAuthor(s)
2 August 2016The common p.R114W HNF4A mutation causes a distinct clinical subtype of monogenic diabetes. Laver, TW; Colclough, K; Shepherd, M; et al.
23 November 2016A principal component meta-analysis on multiple anthropometric traits identifies novel loci for body shape Ried, JS; Jeff M, J; Chu, AY; et al.
1 February 2017Rare and low-frequency coding variants alter human adult height Marouli, E; Graff, M; Medina-Gomez, C; et al.
12 October 2017Cohort profile for the MASTERMIND study: Using the Clinical Practice Research Datalink (CPRD) to investigate stratification of response to treatment in patients with Type 2 diabetes Rodgers, LR; Weedon, MN; Henley, WE; et al.
3 May 2017Dominant ER Stress-Inducing WFS1 Mutations Underlie a Genetic Syndrome of Neonatal/Infancy-Onset Diabetes, Congenital Sensorineural Deafness, and Congenital Cataracts De Franco, E; Flanagan, SE; Yagi, T; et al.
29 June 2016Analysis of cell-free fetal DNA for non-invasive prenatal diagnosis in a family with neonatal diabetes De Franco, E; Caswell, R; Houghton, JA; et al.
9 June 2016Isolated pancreatic aplasia due to a hypomorphic PTF1A mutation Houghton, JA; Swift, GH; Shaw-Smith, C; et al.
6 April 2016Should Studies of Diabetes Treatment Stratification Correct for Baseline HbA1c? Jones, AG; Lonergan, M; Henley, WE; et al.
5 April 2016Type 1 Diabetes Genetic Risk Score: a novel tool to discriminate monogenic and type 1 diabetes Patel, KA; Oram, RA; Flanagan, SE; et al.
11 April 2016Psychiatric morbidity in children with KCNJ11 neonatal diabetes Bowman, P; Broadbridge, E; Knight, BA; et al.
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    Hattersley, AT73
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