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Now showing items 81-87 of 87

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Issue DateTitleAuthor(s)
18 April 2019A specific CNOT1 mutation results in a novel syndrome of pancreatic agenesis and holoprosencephaly through impaired pancreatic and neurological development De Franco, E; Watson, RA; Weninger, WJ; et al.
5 October 2014Defining the role of common variation in the genomic and biological architecture of adult human height. Wood, AR; Esko, T; Yang, J; et al.
1 May 2019Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors Warrington, NM; Beaumont, RN; Horikoshi, M; et al.
5 July 2019Type 1 diabetes genetic risk score discriminates between monogenic and Type 1 diabetes in children diagnosed at the age of < 5 years in the Iranian population Yaghootkar, H; Abbasi, F; Ghaemi, N; et al.
20 October 2019A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin-creatinine ratio. Casanova, F; Tyrrell, J; Beaumont, RN; et al.
16 January 2013Biallelic PDX1 (insulin promoter factor 1) mutations causing neonatal diabetes without exocrine pancreatic insufficiency De Franco, E; Shaw-Smith, C; Flanagan, SE; et al.
6 December 2012GATA6 mutations cause a broad phenotypic spectrum of diabetes from pancreatic agenesis to adult-onset diabetes without exocrine insufficiency De Franco, E; Shaw-Smith, C; Flanagan, SE; et al.
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