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Hsiang-Yu Lin

Showing results (111-120 of 183) with videos related to

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Pediatrics and Neonatology|September 23, 2018
Long-term effects of enzyme replacement therapy for Taiwanese patients with mucopolysaccharidosis IVAHsiang-Yu Lin, Chih-Kuang Chuang, Yu-Yuan Ke, et al.
Molecular Genetics & Genomic Medicine|October 9, 2018
The relationships between urinary glycosaminoglycan levels and phenotypes of mucopolysaccharidosesHsiang-Yu Lin, Chung-Lin Lee, Yun-Ting Lo, et al.
Diagnostics (Basel, Switzerland)|January 8, 2025
Whole Exome Sequencing Facilitates Early Diagnosis of Lesch-Nyhan Syndrome: A Case SeriesHung-Hsiang Fang, Chung-Lin Lee, Hui-Ju Chen, et al.
The Canadian Journal of Cardiology|March 9, 2025
Early Potentially Irreversible Cardiac Damage in Fabry Disease Precedes Gb3 Inclusion Body FormationChung-Lin Lee, Pei-Sin Chen, Yu-Ying Lu, et al.
Annals of Human Genetics|January 5, 2011
Genetic studies of Prader-Willi patients provide evidence for conservation of genomic architecture in proximal chromosome 15qAihua Hou, Shuan-Pei Lin, Shi Yun Ho, et al.
Pediatric Pulmonology|August 19, 2010
Polysomnographic characteristics in patients with mucopolysaccharidosesHsiang-Yu Lin, Ming-Ren Chen, Ching-Chi Lin, et al.
International Journal of Medical Sciences|September 15, 2021
Otorhinolaryngological Management in Taiwanese Patients with MucopolysaccharidosesChung-Lin Lee, Kuo-Sheng Lee, Chih-Kuang Chuang, et al.
Diagnostics (Basel, Switzerland)|August 29, 2024
Genetic and Phenotypic Spectrum of <i>KMT2D</i> Variants in Taiwanese Case Series of Kabuki SyndromeChung-Lin Lee, Chih-Kuang Chuang, Ming-Ren Chen, et al.
Pediatrics and Neonatology|December 25, 2018
Array-CGH increased the diagnostic rate of developmental delay or intellectual disability in TaiwanChung-Lin Lee, Chen-Hao Lee, Chih-Kuang Chuang, et al.
Diagnostics (Basel, Switzerland)|April 26, 2024
Illuminating the Genetic Basis of Congenital Heart Disease in Patients with Kabuki SyndromeChung-Lin Lee, Chih-Kuang Chuang, Ming-Ren Chen, et al.
Pageof 19

Showing results (111-120 of 183) with videos related to

Sort By:
Pageof 19
Pediatrics and Neonatology|September 23, 2018
Long-term effects of enzyme replacement therapy for Taiwanese patients with mucopolysaccharidosis IVAHsiang-Yu Lin, Chih-Kuang Chuang, Yu-Yuan Ke, et al.
Molecular Genetics & Genomic Medicine|October 9, 2018
The relationships between urinary glycosaminoglycan levels and phenotypes of mucopolysaccharidosesHsiang-Yu Lin, Chung-Lin Lee, Yun-Ting Lo, et al.
Diagnostics (Basel, Switzerland)|January 8, 2025
Whole Exome Sequencing Facilitates Early Diagnosis of Lesch-Nyhan Syndrome: A Case SeriesHung-Hsiang Fang, Chung-Lin Lee, Hui-Ju Chen, et al.
The Canadian Journal of Cardiology|March 9, 2025
Early Potentially Irreversible Cardiac Damage in Fabry Disease Precedes Gb3 Inclusion Body FormationChung-Lin Lee, Pei-Sin Chen, Yu-Ying Lu, et al.
Annals of Human Genetics|January 5, 2011
Genetic studies of Prader-Willi patients provide evidence for conservation of genomic architecture in proximal chromosome 15qAihua Hou, Shuan-Pei Lin, Shi Yun Ho, et al.
Pediatric Pulmonology|August 19, 2010
Polysomnographic characteristics in patients with mucopolysaccharidosesHsiang-Yu Lin, Ming-Ren Chen, Ching-Chi Lin, et al.
International Journal of Medical Sciences|September 15, 2021
Otorhinolaryngological Management in Taiwanese Patients with MucopolysaccharidosesChung-Lin Lee, Kuo-Sheng Lee, Chih-Kuang Chuang, et al.
Diagnostics (Basel, Switzerland)|August 29, 2024
Genetic and Phenotypic Spectrum of <i>KMT2D</i> Variants in Taiwanese Case Series of Kabuki SyndromeChung-Lin Lee, Chih-Kuang Chuang, Ming-Ren Chen, et al.
Pediatrics and Neonatology|December 25, 2018
Array-CGH increased the diagnostic rate of developmental delay or intellectual disability in TaiwanChung-Lin Lee, Chen-Hao Lee, Chih-Kuang Chuang, et al.
Diagnostics (Basel, Switzerland)|April 26, 2024
Illuminating the Genetic Basis of Congenital Heart Disease in Patients with Kabuki SyndromeChung-Lin Lee, Chih-Kuang Chuang, Ming-Ren Chen, et al.
Pageof 19