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Genotype-phenotype correlations in children and adolescents with nonclassical congenital adrenal hyperplasia due to 21-hydroxylase deficiency.
Dörr, Helmuth-Günther; Schulze, Nadja; Bettendorf, Markus; Binder, Gerhard; Bonfig, Walter; Denzer, Christian; Dunstheimer, Desiree; Salzgeber, Kirsten; Schmidt, Heinrich; Schwab, Karl Otfried; Voss, Egbert; Wabitsch, Martin; Wölfle, Joachim.
Afiliação
  • Dörr HG; Paediatric Endocrinology, University Children's Hospital, Erlangen, Germany. helmuth-guenther.doerr@uk-erlangen.de.
  • Schulze N; Paediatric Endocrinology, University Children's Hospital, Erlangen, Germany.
  • Bettendorf M; Paediatric Endocrinology, University Children's Hospital, Heidelberg, Germany.
  • Binder G; Paediatric Endocrinology, University Children's Hospital, Tübingen, Germany.
  • Bonfig W; Departement of Paediatrics, Hospital Wels-Grieskirchen, Wels, Austria.
  • Denzer C; Paediatric Endocrinology, University Children's Hospital, Ulm, Germany.
  • Dunstheimer D; University Children's Hospital I, Augsburg, Germany.
  • Salzgeber K; Medical Office, Endokrinologikum, Ulm, Germany.
  • Schmidt H; Paediatric Endocrinology, University Children's Hospital, Munich, Germany.
  • Schwab KO; Paediatric Endocrinology, University Children's Hospital, Freiburg, Germany.
  • Voss E; Departament of Paediatrics, Cnopfsche Kinderklinik, Nuremberg, Germany.
  • Wabitsch M; Paediatric Endocrinology, University Children's Hospital, Ulm, Germany.
  • Wölfle J; Paediatric Endocrinology, University Children's Hospital, Erlangen, Germany.
Mol Cell Pediatr ; 7(1): 8, 2020 Jul 09.
Article em En | MEDLINE | ID: mdl-32647925
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Prognostic_studies Idioma: En Ano de publicação: 2020 Tipo de documento: Article