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Mei-Chyn Chao

Showing results (61-70 of 65) with videos related to

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Diagnostics (Basel, Switzerland)|October 16, 2025
Functional Independence Assessment in Children and Adolescents with Achondroplasia: A Multicenter Cross-Sectional Study Using the WeeFIM ScaleChung-Lin Lee, Hung-Hsiang Fang, Chih-Kuang Chuang, et al.
Journal of Personalized Medicine|November 27, 2021
Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver-Russell SyndromeHsiang-Yu Lin, Chung-Lin Lee, Sisca Fran, et al.
International Journal of Medical Sciences|January 2, 2024
Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Silver-Russell SyndromeHsiang-Yu Lin, Chung-Lin Lee, Yuan-Rong Tu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 24, 2013
Plasma globotriaosylsphingosine (lysoGb3) could be a biomarker for Fabry disease with a Chinese hotspot late-onset mutation (IVS4+919G>A)Hsuan-Chieh Liao, Yu-Hsiu Huang, Yann-Jang Chen, et al.
In Vivo (Athens, Greece)|December 26, 2023
Spectrum of PHEX Mutations and FGF23 Profiles in a Taiwanese Cohort With X-Linked Hypophosphatemia Including 102 PatientsPen-Hua Su, Ju-Shan Yu, Yu-Zhen Wu, et al.
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Showing results (61-70 of 65) with videos related to

Sort By:
Pageof 7
You have reached the last page of results.This site can display upto 65 results.
Diagnostics (Basel, Switzerland)|October 16, 2025
Functional Independence Assessment in Children and Adolescents with Achondroplasia: A Multicenter Cross-Sectional Study Using the WeeFIM ScaleChung-Lin Lee, Hung-Hsiang Fang, Chih-Kuang Chuang, et al.
Journal of Personalized Medicine|November 27, 2021
Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver-Russell SyndromeHsiang-Yu Lin, Chung-Lin Lee, Sisca Fran, et al.
International Journal of Medical Sciences|January 2, 2024
Quantitative DNA Methylation Analysis and Epigenotype-Phenotype Correlations in Taiwanese Patients with Silver-Russell SyndromeHsiang-Yu Lin, Chung-Lin Lee, Yuan-Rong Tu, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|September 24, 2013
Plasma globotriaosylsphingosine (lysoGb3) could be a biomarker for Fabry disease with a Chinese hotspot late-onset mutation (IVS4+919G>A)Hsuan-Chieh Liao, Yu-Hsiu Huang, Yann-Jang Chen, et al.
In Vivo (Athens, Greece)|December 26, 2023
Spectrum of PHEX Mutations and FGF23 Profiles in a Taiwanese Cohort With X-Linked Hypophosphatemia Including 102 PatientsPen-Hua Su, Ju-Shan Yu, Yu-Zhen Wu, et al.
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