Genetic analyses in a cohort of pediatric patients with congenital hypothyroidism based on congenital hypothyroidism consensus guideline.

Kurnaz E., Türkyılmaz A., Yaralı O., Dönmez A. S., Çayır A.

Hormone research in paediatrics, cilt.99, sa.1, ss.23-37, 2026 (SCI-Expanded, Scopus) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: 99 Sayı: 1
  • Basım Tarihi: 2026
  • Doi Numarası: 10.1159/000541898
  • Dergi Adı: Hormone research in paediatrics
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus, Academic Search Premier, BIOSIS, CAB Abstracts, Chemical Abstracts Core, EMBASE, Food Science & Technology Abstracts, MEDLINE, SportDiscus
  • Sayfa Sayıları: ss.23-37
  • Anahtar Kelimeler: Congenital hypothyroidism, Gene mutation analysis, NKX2-1-related disorders, Thyroid dysgenesis, Thyroid dyshormonogenesis
  • Karadeniz Teknik Üniversitesi Adresli: Evet