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Query Trace: Birth Weight and HNF4A[original query]

The Common p.R114W HNF4A Mutation Causes a Distinct Clinical Subtype of Monogenic Diabetes. Diabetes 2016 Aug . Laver Thomas W, Colclough Kevin, Shepherd Maggie, Patel Kashyap, Houghton Jayne Al, Dusatkova Petra, Pruhova Stepanka, Morris Andrew D, Palmer Colin N, McCarthy Mark I, Ellard Sian, Hattersley Andrew T, Weedon Michael Similar articles in PubMed
Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations. European journal of endocrinology / European Federation of Endocrine Societies 2010 May 162 (5): 987-92. Flanagan S E, Kapoor R R, Mali G, Cody D, Murphy N, Schwahn B, Siahanidou T, Banerjee I, Akcay T, Rubio-Cabezas O, Shield J P H, Hussain K, Ellard Similar articles in PubMed
Genetic variation in the small heterodimer partner gene and young-onset type 2 diabetes, obesity, and birth weight in U.K. subjects. Diabetes 2003 May 52 (5): 1276-9. Mitchell Simon M S, Weedon Michael N, Owen Katharine R, Shields Beverley, Wilkins-Wall Beverley, Walker Mark, McCarthy Mark I, Frayling Timothy M, Hattersley Andrew Similar articles in PubMed