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A Novel TBX19 Gene Mutation in a Case of Congenital Isolated Adrenocorticotropic Hormone Deficiency Presenting with Recurrent Respiratory Tract Infections.
Akcan, Nese; Serakinci, Nedime; Turkgenc, Burcu; Bundak, Ruveyde; Bahceciler, Nerin; Temel, Sehime G.
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  • Akcan N; Faculty of Medicine, Department of Pediatric Endocrinology, University of Near East, Nicosia, Cyprus.
  • Serakinci N; Faculty of Medicine, Department of Medical Genetics, University of Near East, Nicosia, Cyprus.
  • Turkgenc B; Genetic Diagnostic Center, University of Acibadem, Istanbul, Turkey.
  • Bundak R; Faculty of Medicine, Department of Pediatric Endocrinology, University of Kyrenia, Kyrenia, Cyprus.
  • Bahceciler N; Faculty of Medicine, Department of Pediatric Allergy and Immunology, University of Near East, Nicosia, Cyprus.
  • Temel SG; Faculty of Medicine, Department of Histology and Embryology, University of Near East, Nicosia, Cyprus.
Front Endocrinol (Lausanne) ; 8: 64, 2017.
Article en En | MEDLINE | ID: mdl-28458651
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Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Endocrinol (Lausanne) Año: 2017 Tipo del documento: Article País de afiliación: Chipre
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Bases de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Front Endocrinol (Lausanne) Año: 2017 Tipo del documento: Article País de afiliación: Chipre