Ann Pediatr Endocrinol Metab Search

CLOSE


Search

  • HOME
  • Search
Molecular basis and genetic testing strategies for diagnosing 21-hydroxylase deficiency, including CAH-X syndrome
Ja Hye Kim, Gu-Hwan Kim, Han-Wook Yoo, Jin-Ho Choi
Ann Pediatr Endocrinol Metab. 2023;28(2):77-86.   Published online June 30, 2023
Full textFull text    PubreaderPubReader    ePubePub    CrossRef-TDMCrossref - TDM    PDFPDF    
Recent advances in biochemical and molecular analysis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency
Jin-Ho Choi, Gu-Hwan Kim, Han-Wook Yoo
Ann Pediatr Endocrinol Metab. 2016;21(1):1-6.   Published online March 31, 2016
Full textFull text    PubreaderPubReader    ePubePub    CrossRef-TDMCrossref - TDM    PDFPDF    
Genotype of Steroid 21-Hydroxylase Gene and Clinical Characteristics in Patients with Congenital Adrenal Hyperplasia 21-Hydroxylase Deficiency.
Jung Min Ko, Jin Ho Choi, Gu Hwan Kim, Han Wook Yoo
Ann Pediatr Endocrinol Metab. 2005;10(1):57-63.
PDFPDF    
  • Journal Impact Factor 2.2
  • SCImago Journal & Country Rank
  • templates


ABOUT
ARTICLE CATEGORY

Browse all articles >

BROWSE ARTICLES
AUTHOR INFORMATION
Editorial Office
501-107, 30 Seocho-daero 74-gil, Seocho-gu, Seoul 06622, Republic of Korea
Tel: +82-2-3471-4268    Fax: +82-2-3471-4269    E-mail: kspe.editor@gmail.com                

Copyright © 2023 by Korean Society of Pediatric Endocrinology.

Developed in M2PI

Close layer
prev next