Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single center-Reference-Cited by-同舟云学术

Genotype-phenotype correlation in 27 pediatric patients in congenital adrenal hyperplasia due to 21-hydroxylase deficiency in a single center

Author:

Yoo Yangho¹,Chang Mi Sun¹,Lee Jieun¹,Cho Sung Yoon²,Park Sung Won³,Jin Dong-Kyu¹,Park Hyung-Doo⁴

Affiliation:

1. Department of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

2. Department of Pediatrics, Hanyang University Guri Hopistal, Hanyang University College of Medicine, Guri, Korea.

3. Department of Pediatrics, Cheil General Hospital & Woman's Healthcare Center, Kwandong University College of Medicine, Seoul, Korea.

4. Department of Laboratory Medicine and Genetics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.

Publisher

Korean Society of Pediatric Endocrinology

Subject

Endocrinology, Diabetes and Metabolism,Pediatrics, Perinatology, and Child Health

Link

Reference39 articles.

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