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Molecular spectrum of TSHß subunit gene defects in central hypothyroidism in the UK and Ireland.
Nicholas, A K; Jaleel, S; Lyons, G; Schoenmakers, E; Dattani, M T; Crowne, E; Bernhard, B; Kirk, J; Roche, E F; Chatterjee, V K; Schoenmakers, N.
Afiliação
  • Nicholas AK; University of Cambridge Metabolic Research Laboratories, Wellcome Trust-Medical Research Council Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, UK.
  • Jaleel S; Department of Paediatric Endocrinology & Diabetes, National Children's Hospital, AMNCH, Dublin, Ireland.
  • Lyons G; University of Cambridge Metabolic Research Laboratories, Wellcome Trust-Medical Research Council Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, UK.
  • Schoenmakers E; University of Cambridge Metabolic Research Laboratories, Wellcome Trust-Medical Research Council Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, UK.
  • Dattani MT; University College London Institute of Child Health, Developmental Endocrinology Research Group, Section of Genetics and Epigenetics in Health and Disease, Genetics and Genomic Medicine Programme, London, UK.
  • Crowne E; Department of Paediatric Endocrinology & Diabetes, Bristol Royal Hospital for Children, University Hospitals Bristol NHS Foundation Trust, Bristol, UK.
  • Bernhard B; Department of Clinical Genetics, North West Thames Regional Genetics Service, North West London Hospitals NHS Trust, Harrow, UK.
  • Kirk J; Department of Endocrinology, Birmingham Children's Hospital, Birmingham, UK.
  • Roche EF; Department of Paediatric Endocrinology & Diabetes, National Children's Hospital, AMNCH, Dublin, Ireland.
  • Chatterjee VK; University of Dublin, Trinity College Dublin, Dublin, Ireland.
  • Schoenmakers N; University of Cambridge Metabolic Research Laboratories, Wellcome Trust-Medical Research Council Institute of Metabolic Science, Addenbrooke's Hospital, Cambridge, UK.
Clin Endocrinol (Oxf) ; 86(3): 410-418, 2017 Mar.
Article em En | MEDLINE | ID: mdl-27362444
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Triagem Neonatal / Hipotireoidismo Congênito / Tireotropina Subunidade beta Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male / Newborn País/Região como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article
Texto completo
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Triagem Neonatal / Hipotireoidismo Congênito / Tireotropina Subunidade beta Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Female / Humans / Male / Newborn País/Região como assunto: Europa Idioma: En Ano de publicação: 2017 Tipo de documento: Article