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Dau-Ming Niu

Showing results (181-190 of 184) with videos related to

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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.
Journal of the American College of Cardiology|December 10, 2016
Later Onset Fabry Disease, Cardiac Damage Progress in Silence: Experience With a Highly Prevalent MutationTing-Rong Hsu, Sheng-Che Hung, Fu-Pang Chang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2025
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
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Showing results (181-190 of 184) with videos related to

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Pageof 19
You have reached the last page of results.This site can display upto 184 results.
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.
Journal of the American College of Cardiology|December 10, 2016
Later Onset Fabry Disease, Cardiac Damage Progress in Silence: Experience With a Highly Prevalent MutationTing-Rong Hsu, Sheng-Che Hung, Fu-Pang Chang, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 13, 2025
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
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