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Challenges of CYP21A2 genotyping in children with 21-hydroxylase deficiency: determination of genotype-phenotype correlation using next generation sequencing in Southeastern Anatolia.
Karaoglan, M; Nacarkahya, G; Aytaç, E H; Keskin, M.
Affiliation
  • Karaoglan M; Department of Pediatric Endocrinology, Gaziantep University Faculty of Medicine, Gaziantep, Turkey. muratkaraoglan@gantep.edu.tr.
  • Nacarkahya G; Department of Molecular Biology, Gaziantep University Faculty of Medicine, Gaziantep, Turkey.
  • Aytaç EH; Department of Pediatric Endocrinology, Gaziantep University Faculty of Medicine, Gaziantep, Turkey.
  • Keskin M; Department of Pediatric Endocrinology, Gaziantep University Faculty of Medicine, Gaziantep, Turkey.
J Endocrinol Invest ; 44(11): 2395-2405, 2021 Nov.
Article in En | MEDLINE | ID: mdl-33677812
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virilism / Water-Electrolyte Imbalance / Steroid 21-Hydroxylase / Adrenal Hyperplasia, Congenital / Genetic Association Studies Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Adolescent / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: J Endocrinol Invest Year: 2021 Type: Article Affiliation country: Turkey
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Virilism / Water-Electrolyte Imbalance / Steroid 21-Hydroxylase / Adrenal Hyperplasia, Congenital / Genetic Association Studies Type of study: Diagnostic_studies / Etiology_studies / Prognostic_studies Limits: Adolescent / Female / Humans / Male Country/Region as subject: Asia Language: En Journal: J Endocrinol Invest Year: 2021 Type: Article Affiliation country: Turkey