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Chromosome 17q12 microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorder.
Clissold, Rhian L; Shaw-Smith, Charles; Turnpenny, Peter; Bunce, Benjamin; Bockenhauer, Detlef; Kerecuk, Larissa; Waller, Simon; Bowman, Pamela; Ford, Tamsin; Ellard, Sian; Hattersley, Andrew T; Bingham, Coralie.
Afiliación
  • Clissold RL; University of Exeter Medical School, Exeter, UK; National Institute for Health Research Exeter Clinical Research Facility, Royal Devon and Exeter National Health Service Foundation Trust, Exeter, UK.
  • Shaw-Smith C; Clinical Genetics Department, Royal Devon and Exeter National Health Service Foundation Trust, Exeter, UK.
  • Turnpenny P; Clinical Genetics Department, Royal Devon and Exeter National Health Service Foundation Trust, Exeter, UK.
  • Bunce B; Department of Molecular Genetics, Royal Devon and Exeter National Health Service Foundation Trust, Exeter, UK.
  • Bockenhauer D; Department of Nephrology, Great Ormond Street Hospital for Children National Health Service Foundation Trust, London, UK; University College of London Centre for Nephrology, London, UK.
  • Kerecuk L; Department of Nephrology, Birmingham Children's Hospital, Birmingham, UK.
  • Waller S; Department of Nephrology, Evelina London Children's Hospital, St. Thomas' Hospital, London, UK.
  • Bowman P; University of Exeter Medical School, Exeter, UK.
  • Ford T; University of Exeter Medical School, Exeter, UK.
  • Ellard S; University of Exeter Medical School, Exeter, UK; Department of Molecular Genetics, Royal Devon and Exeter National Health Service Foundation Trust, Exeter, UK.
  • Hattersley AT; University of Exeter Medical School, Exeter, UK; National Institute for Health Research Exeter Clinical Research Facility, Royal Devon and Exeter National Health Service Foundation Trust, Exeter, UK; Macleod Diabetes and Endocrine Centre, Royal Devon and Exeter National Health Service Foundation Tru
  • Bingham C; University of Exeter Medical School, Exeter, UK; Exeter Kidney Unit, Royal Devon and Exeter National Health Service Foundation Trust, Exeter, UK. Electronic address: c.bingham@exeter.ac.uk.
Kidney Int ; 90(1): 203-11, 2016 07.
Article en En | MEDLINE | ID: mdl-27234567
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 17 / Eliminación de Secuencia / Factor Nuclear 1-beta del Hepatocito / Trastornos del Neurodesarrollo / Enfermedades Renales Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Kidney Int Año: 2016 Tipo del documento: Article País de afiliación: Reino Unido
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Cromosomas Humanos Par 17 / Eliminación de Secuencia / Factor Nuclear 1-beta del Hepatocito / Trastornos del Neurodesarrollo / Enfermedades Renales Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Child / Female / Humans / Male / Middle aged Idioma: En Revista: Kidney Int Año: 2016 Tipo del documento: Article País de afiliación: Reino Unido