Clinical, biochemical and genetic features with nonclassical 21-hydroxylase deficiency and final height


SAVAS-ERDEVE S., CETINKAYA S., Abali Z. Y. , Poyrazoglu S. , Bas F. , Berberoglu M., ...Daha Fazla

JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, cilt.30, ss.759-766, 2017 (SCI İndekslerine Giren Dergi) identifier identifier identifier

  • Cilt numarası: 30 Konu: 7
  • Basım Tarihi: 2017
  • Doi Numarası: 10.1515/jpem-2017-0088
  • Dergi Adı: JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
  • Sayfa Sayıları: ss.759-766

Özet

Background: The clinical, laboratory, genetic properties and final height of a large cohort of patients with nonclassical 21-hydroxylase deficiency (NC21OHD) in Turkey were analyzed.