Mild and severe congenital primary hypothyroidism in two patients by thyrotropin receptor (TSHR) gene mutation.

Baş V. N. , Cangul H., Agladioglu S., Kendall M., Cetinkaya S., Maher E., ...More

Journal of pediatric endocrinology & metabolism : JPEM, vol.25, pp.1153-6, 2012 (Peer-Reviewed Journal) identifier identifier identifier

  • Publication Type: Article / Article
  • Volume: 25
  • Publication Date: 2012
  • Doi Number: 10.1515/jpem-2012-0211
  • Journal Name: Journal of pediatric endocrinology & metabolism : JPEM
  • Journal Indexes: Science Citation Index Expanded, Scopus
  • Page Numbers: pp.1153-6