Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single center
Yangho Yoo, Mi Sun Chang, Jieun Lee, Sung Yoon Cho, Sung Won Park, Dong-Kyu Jin, Hyung-Doo Park
Ann Pediatr Endocrinol Metab. 2013;18(3):128-134.   Published online 2013 Sep 30     DOI:
Citations to this article as recorded by Crossref logo
The distribution of intrafamilial CYP21A2 mutant alleles and investigation of clinical features in Turkish children and their siblings in Southeastern Anatolia
Murat Karaoglan
Journal of Pediatric Endocrinology and Metabolism.2019; 32(12): 1311.     CrossRef
Biology of the Adrenal Gland Cortex Obviates Effective Use of Adeno-Associated Virus Vectors to Treat Hereditary Adrenal Disorders
Sandra Markmann, Bishnu P. De, Jasmine Reid, Clarisse L. Jose, Jonathan B. Rosenberg, Philip L. Leopold, Stephen M. Kaminsky, Dolan Sondhi, Odelya Pagovich, Ronald G. Crystal
Human Gene Therapy.2018; 29(4): 403.     CrossRef
Congenital Adrenal Hyperplasia with Non-functional Mutations in Both Alleles in a Clinically Unaffected Infant
Thomas Hoehn, Zoltan Lukacs, Wolfgang Huckenbeck, Toni Torresani, Oliver Blankenstein, Saysanasongkham Bounnack
Journal of Tropical Pediatrics.2016; 62(2): 158.     CrossRef
CYP21A2Mutation Analysis in Korean Patients With Congenital Adrenal Hyperplasia Using Complementary Methods: Sequencing After Long-Range PCR and Restriction Fragment Length Polymorphism Analysis With Multiple Ligation-Dependent Probe Amplification Assay
Geehay Hong, Hyung-Doo Park, Rihwa Choi, Dong-Kyu Jin, Jae Hyeon Kim, Chang-Seok Ki, Soo-Youn Lee, Junghan Song, Jong-Won Kim
Annals of Laboratory Medicine.2015; 35(5): 535.     CrossRef