A rare combination: congenital adrenal hyperplasia due to 21 hydroxylase deficiency and Turner syndrome.


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Kendirci H., Aycan Z., Çetinkaya S., Baş V. N. , Ağladıoğlu S., Önder A.

Journal of clinical research in pediatric endocrinology, vol.4, pp.213-5, 2012 (Peer-Reviewed Journal) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 4
  • Publication Date: 2012
  • Doi Number: 10.4274/jcrpe.767
  • Journal Name: Journal of clinical research in pediatric endocrinology
  • Journal Indexes: Science Citation Index Expanded, Scopus
  • Page Numbers: pp.213-5