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Genetic diagnosis of congenital hypopituitarism in Turkish patients by a target gene panel: novel pathogenic variants in GHRHR, GLI2, LHX4 and POU1F1 genes.
Kirkgöz, Tarik; Gürsoy, Semra; Acar, Sezer; Nalbantoglu, Özlem; Özkaya, Beyhan; Anil Korkmaz, Hüseyin; Hazan, Filiz; Özkan, Behzat.
Afiliación
  • Kirkgöz T; Division of Pediatric Endocrinology, Dr. Behçet Uz Children's Education and Research Hospital, Izmir, Turkey, tarikkrkgz@gmail.com.
  • Gürsoy S; Division of Pediatric Genetics, Dr. Behçet Uz Children's Education and Research Hospital, Izmir, Turkey.
  • Acar S; Division of Pediatric Endocrinology, Dr. Behçet Uz Children's Education and Research Hospital, Izmir, Turkey.
  • Nalbantoglu Ö; Division of Pediatric Endocrinology, Dr. Behçet Uz Children's Education and Research Hospital, Izmir, Turkey.
  • Özkaya B; Division of Pediatric Endocrinology, Dr. Behçet Uz Children's Education and Research Hospital, Izmir, Turkey.
  • Anil Korkmaz H; Division of Pediatric Endocrinology, Dr. Behçet Uz Children's Education and Research Hospital, Izmir, Turkey.
  • Hazan F; Department of Medical Genetics, Dr. Behçet Uz Children's Education and Research Hospital, Izmir, Turkey.
  • Özkan B; Division of Pediatric Endocrinology, Dr. Behçet Uz Children's Education and Research Hospital, Izmir, Turkey.
Arch Endocrinol Metab ; 68: e220254, 2023 Nov 10.
Article en En | MEDLINE | ID: mdl-37948564
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Hipopituitarismo Límite: Female / Humans / Male Idioma: En Revista: Arch Endocrinol Metab Año: 2023 Tipo del documento: Article
Texto completo
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Hipopituitarismo Límite: Female / Humans / Male Idioma: En Revista: Arch Endocrinol Metab Año: 2023 Tipo del documento: Article