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Now showing items 81-87 of 87

Issue Date	Title	Author(s)
18 April 2019	A 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 2014	Defining 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 2019	Maternal 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 2019	Type 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 2019	A genome-wide association study implicates multiple mechanisms influencing raised urinary albumin-creatinine ratio.	Casanova, F; Tyrrell, J; Beaumont, RN; et al.
16 January 2013	Biallelic 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 2012	GATA6 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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