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Evaluation of growth and puberty in a child with a novel TBX19 gene mutation and review of the literature.
Abali, Zehra Yavas; Yesil, Gozde; Kirkgoz, Tarik; Kaygusuz, Sare Betul; Eltan, Mehmet; Turan, Serap; Bereket, Abdullah; Guran, Tulay.
Affiliation
  • Abali ZY; Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Istanbul, Turkey.
  • Yesil G; Department of Medical Genetics, Bezmialem Vakif University School of Medicine, Istanbul, Turkey.
  • Kirkgoz T; Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Istanbul, Turkey.
  • Kaygusuz SB; Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Istanbul, Turkey.
  • Eltan M; Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Istanbul, Turkey.
  • Turan S; Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Istanbul, Turkey.
  • Bereket A; Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Istanbul, Turkey.
  • Guran T; Department of Pediatric Endocrinology and Diabetes, Marmara University School of Medicine, Istanbul, Turkey. tulayguran@yahoo.com.
Hormones (Athens) ; 18(2): 229-236, 2019 Jun.
Article de En | MEDLINE | ID: mdl-30747411
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Développement de l'enfant / Puberté / Hormone corticotrope / Protéines à homéodomaine / Protéines à domaine boîte-T / Maladies endocriniennes / Maladies génétiques congénitales / Hypoglycémie Type d'étude: Etiology_studies Limites: Child, preschool / Female / Humans Langue: En Journal: Hormones (Athens) Sujet du journal: ENDOCRINOLOGIA Année: 2019 Type de document: Article Pays d'affiliation: Turquie Pays de publication: Suisse
Texte intégral
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XML
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Développement de l'enfant / Puberté / Hormone corticotrope / Protéines à homéodomaine / Protéines à domaine boîte-T / Maladies endocriniennes / Maladies génétiques congénitales / Hypoglycémie Type d'étude: Etiology_studies Limites: Child, preschool / Female / Humans Langue: En Journal: Hormones (Athens) Sujet du journal: ENDOCRINOLOGIA Année: 2019 Type de document: Article Pays d'affiliation: Turquie Pays de publication: Suisse