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Orphanet Journal of Rare Diseases|September 15, 2023
Changing clinical manifestations of Gaucher disease in TaiwanWen-Li Lu, Yin-Hsiu Chien, Fuu-Jen Tsai, et al.
Molecular Genetics and Metabolism|May 25, 2016
3-O-methyldopa levels in newborns: Result of newborn screening for aromatic l-amino-acid decarboxylase deficiencyYin-Hsiu Chien, Pin-Wen Chen, Ni-Chung Lee, et al.
Medical Teacher|October 14, 2024
Can routine EPA-based assessments predict OSCE performances of undergraduate medical students?Yi-Hsuan Lin, Ying-Ying Yang, Chen-Huan Chen, et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi|February 27, 2018
Congenital generalized lipodystrophy in TaiwanRai-Hseng Hsu, Wei-De Lin, Mei-Chyn Chao, et al.
Diagnostics (Basel, Switzerland)|May 14, 2025
Functional Independence of Taiwanese Children with Silver-Russell SyndromeHung-Hsiang Fang, Chung-Lin Lee, Chih-Kuang Chuang, et al.
American Journal of Medical Genetics. Part A|December 15, 2019
Cardiac manifestations and gene mutations of patients with RASopathies in TaiwanChung-Lin Lee, Louis Tan Hock-Cheong Tan, Hsiang-Yu Lin, et al.
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