Showing 1 - 3 results of 3 for search 'Kevin Colclough', query time: 0.02s Refine Results
  1. 1
    Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases

    Expanding the Phenotype of TRMT10A Mutations: Case Report and a Review of the Existing Cases by Zeynep Şıklar, Tuğba Kontbay, Kevin Colclough, Kashyap A. Patel, Merih Berberoğlu

    Published 2023
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  2. 2
    Case report: adult onset diabetes with partial pancreatic agenesis and congenital heart disease due to a de novo GATA6 mutation

    Case report: adult onset diabetes with partial pancreatic agenesis and congenital heart disease due to a de novo GATA6 mutation by Begona Sanchez-Lechuga, Muhammad Saqlain, Nicholas Ng, Kevin Colclough, Conor Woods, Maria Byrne

    Published 2020
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  3. 3
    Heterozygous Insulin Receptor <italic>(INSR)</italic> Mutation Associated with Neonatal Hyperinsulinemic Hypoglycaemia and Familial Diabetes Mellitus: Case Series

    Heterozygous Insulin Receptor <italic>(INSR)</italic> Mutation Associated with Neonatal Hyperinsulinemic Hypoglycaemia and Familial Diabetes Mellitus: Case Series by Aashish Sethi, Nicola Foulds, Sarah Ehtisham, Syed Haris Ahmed, Jayne Houghton, Kevin Colclough, Mohammed Didi, Sarah E. Flanagan, Senthil Senniappan

    Published 2020
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