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Analysis of ProP1 Gene in a Cohort of Tunisian Patients with Congenital Combined Pituitary Hormone Deficiency.
Moalla, Mariam; Mnif-Feki, Mouna; Safi, Wajdi; Charfi, Nadia; Mejdoub-Rekik, Nabila; Abid, Mohamed; Hadj Kacem, Faten; Hadj Kacem, Hassen.
Afiliação
  • Moalla M; Laboratory of Molecular and Cellular Screening Processes, Center of Biotechnology of Sfax, Sfax 3018, Tunisia.
  • Mnif-Feki M; Laboratory of Human Molecular Genetics, Faculty of Medicine of Sfax, University of Sfax, Sfax 3029, Tunisia.
  • Safi W; Endocrinology Department, Hedi Chaker Hospital, Sfax 3029, Tunisia.
  • Charfi N; Endocrinology Department, Hedi Chaker Hospital, Sfax 3029, Tunisia.
  • Mejdoub-Rekik N; Endocrinology Department, Hedi Chaker Hospital, Sfax 3029, Tunisia.
  • Abid M; Endocrinology Department, Hedi Chaker Hospital, Sfax 3029, Tunisia.
  • Hadj Kacem F; Endocrinology Department, Hedi Chaker Hospital, Sfax 3029, Tunisia.
  • Hadj Kacem H; Endocrinology Department, Hedi Chaker Hospital, Sfax 3029, Tunisia.
J Clin Med ; 11(24)2022 Dec 19.
Article em En | MEDLINE | ID: mdl-36556141
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Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Clin Med Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Tunísia
Texto completo
Adicionar na Minha BVS
Imprimir
XML
PubMed Links
Buscar no Google

Texto completo: 1 Bases de dados: MEDLINE Tipo de estudo: Prognostic_studies / Risk_factors_studies Idioma: En Revista: J Clin Med Ano de publicação: 2022 Tipo de documento: Article País de afiliação: Tunísia