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Identification of a novel mutation of the
SHOX
gene in a patient with Leri-Weill dyschondrosteosis accompanied by growth hormone deficiency
Jaebeen Kang
, Min-Ji Kim
, Sukdong Yoo
, Chong Kun Cheon
Ann Pediatr Endocrinol Metab.
2024;29(3):201-203. Published online June 30, 2024
DOI:
https://doi.org/10.6065/apem.2346236.118
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Journal Impact Factor 2.8
Pediatrics Q1
ABOUT
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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
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