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17q12 Deletion Syndrome as a Rare Cause for Diabetes Mellitus Type MODY5.
Roehlen, Natascha; Hilger, Hanna; Stock, Friedrich; Gläser, Birgitta; Guhl, Johannes; Schmitt-Graeff, Annette; Seufert, Jochen; Laubner, Katharina.
Afiliação
  • Roehlen N; Division of Endocrinology and Diabetology, Department of Medicine II, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Hilger H; Division of Endocrinology and Diabetology, Department of Medicine II, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Stock F; Institute of Human Genetics, Medical Faculty, University of Freiburg, Freiburg, Germany.
  • Gläser B; Institute of Human Genetics, Medical Faculty, University of Freiburg, Freiburg, Germany.
  • Guhl J; General Practice and Family Medicine, Villingen-Schwenningen, Germany.
  • Schmitt-Graeff A; Institute for Clinical Pathology, Medical Faculty, University of Freiburg, Freiburg, Germany.
  • Seufert J; Division of Endocrinology and Diabetology, Department of Medicine II, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Laubner K; Division of Endocrinology and Diabetology, Department of Medicine II, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
J Clin Endocrinol Metab ; 103(10): 3601-3610, 2018 10 01.
Article em En | MEDLINE | ID: mdl-30032214

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 17 / Doenças do Sistema Nervoso Central / Deleção Cromossômica / Esmalte Dentário / Diabetes Mellitus Tipo 2 / Doenças Renais Císticas / Fator 1-beta Nuclear de Hepatócito Limite: Adolescent / Adult / Female / Humans Idioma: En Revista: J Clin Endocrinol Metab Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Cromossomos Humanos Par 17 / Doenças do Sistema Nervoso Central / Deleção Cromossômica / Esmalte Dentário / Diabetes Mellitus Tipo 2 / Doenças Renais Císticas / Fator 1-beta Nuclear de Hepatócito Limite: Adolescent / Adult / Female / Humans Idioma: En Revista: J Clin Endocrinol Metab Ano de publicação: 2018 Tipo de documento: Article País de afiliação: Alemanha País de publicação: Estados Unidos