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An update on the genetic causes of central precocious puberty
Young-Lim Shin
Ann Pediatr Endocrinol Metab.
2016;21(2):66-69. Published online June 30, 2016
DOI:
https://doi.org/10.6065/apem.2016.21.2.66
Crossref 27
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Resistance to thyroid hormone due to a novel mutation of thyroid hormone receptor beta gene
Jae Hee Lee, Eun Young Kim
Ann Pediatr Endocrinol Metab.
2014;19(4):229-231. Published online December 31, 2014
DOI:
https://doi.org/10.6065/apem.2014.19.4.229
Crossref 10
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A novel
de novo
mutation within
PHEX
gene in a young girl with hypophosphatemic rickets and review of literature
Chong Kun Cheon, Hoon Sang Lee, Su Yung Kim, Min Jung Kwak, Gu-Hwan Kim, Han-Wook Yoo
Ann Pediatr Endocrinol Metab.
2014;19(1):36-41. Published online March 31, 2014
DOI:
https://doi.org/10.6065/apem.2014.19.1.36
Crossref 8
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A Novel Mutation of the Steroid 5-Alpha Reductase Type 2 (SRD5A2) Gene in a Korean Newborn with Ambiguous Genitalia.
Ran Hee Kim, Su Yung Kim, Han Wook Yoo, Gu Hwan Kim, Chong Kun Cheon
Ann Pediatr Endocrinol Metab.
2010;15(2):133-137.
PDF
Hypogonadotropic Hypogonadism and Abnormal Olfactory Bulb Development in CHARGE Syndrome with CHD7 Mutation.
Sun Hyang Lee, Yong Wha Lee, Young Lim Shin
Ann Pediatr Endocrinol Metab.
2009;14(1):68-72.
PDF
A Familial Case of Idiopathic Hypogonadotropic Hypogonadism Occurred in a Boy and His Sister.
Eun Jung Yoo, Kyoung Sim Kim, Yong Wook Kim, Han Wook Yoo, Eun Young Kim
Ann Pediatr Endocrinol Metab.
2006;11(2):199-204.
PDF
Mutational Analysis of PTPN11 Gene in Noonan Syndrome.
Sung Yeon Ahn, Choong Ho Shin, Sei Won Yang
Ann Pediatr Endocrinol Metab.
2005;10(2):188-194.
PDF
Plasma Ghrelin Levels and Its Relationship with Obesity in Obese Children.
Dae Sun Jo, Jae Un Lee, Sun Young Kim, Sun Jun Kim, Chang Won Kang, Pyoung Han Hwang, Dae Yeol Lee
Ann Pediatr Endocrinol Metab.
2004;9(2):179-185.
PDF
Genetic Analysis in a Case of Transient Neonatal Diabetes Mellitus with Congenital Adrenal Hyperplasia.
Hye Jin Kwon, Jin A Park, Sang Lack Lee, Heung Sik Kim, Dong Seok Jeon, Dong Kyu Jin, Pyoung Han Hwang
Ann Pediatr Endocrinol Metab.
2002;7(1):116-121.
PDF
Three Cases of Congenital Adrenal Hyperplasia Owing to Multiple Mutations of CYP21 Gene.
Jun Heo, Jae Hong Yu, Dong Ki Jeong
Ann Pediatr Endocrinol Metab.
2001;6(2):176-181.
PDF
Screening for Mitochondrial DNA Mutations of MELAS tRNA Leu(3243), MERRF tRNA Lys(8344) in Korean IDDM Patients.
Han Wook Yoo
Ann Pediatr Endocrinol Metab.
1997;2(2):233-240.
PDF
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Journal Impact Factor 2.8
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ABOUT
Aims and Scope
About the Journal
Editorial Board
Principles of Transparency and Best Practice
Open Access
Subscription Information
Contact us
ARTICLE CATEGORY
Original Article
Review Article
Case Report
Others
Browse all articles >
BROWSE ARTICLES
New Issue
All Issues
Accepted
Ahead-of Print
Most View
Most Download
Most Cited
Funded Articles
Author Index
AUTHOR INFORMATION
Instructions for Authors
Research and Publication Ethics
Readership
Advertising policies
Article-processing Charge
Author’s Checklist
E-Submission
Copyright Transfer Agreement