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Li-Ping Tsai

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Acta Paediatrica (Oslo, Norway : 1992)|June 1, 2007
Genotype and phenotype in patients with Prader-Willi syndrome in TaiwanHsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang, et al.
Pediatrics and Neonatology|September 12, 2012
A novel 3670-base pair mitochondrial DNA deletion resulting in multi-systemic manifestations in a childHsin-Ming Liu, Li-Ping Tsai, Yin-Hsiu Chien, et al.
American Journal of Medical Genetics. Part A|April 28, 2009
Incidence of the mucopolysaccharidoses in Taiwan, 1984-2004Hsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang, et al.
American Journal of Medical Genetics. Part A|April 27, 2018
Functional independence of Taiwanese children with Prader-Willi syndromeChung-Lin Lee, Hsiang-Yu Lin, Li-Ping Tsai, et al.
Journal of the Chinese Medical Association : JCMA|June 24, 2008
Effects of growth hormone treatment on height, weight, and obesity in Taiwanese patients with Prader-Willi syndromeHsiang-Yu Lin, Shuan-Pei Lin, Li-Ping Tsai, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 30, 2007
Prader-Willi syndrome in TaiwanHsiang-Yu Lin, Shuan-Pei Lin, Jui-Lung Yen, et al.
The Journal of Clinical Endocrinology and Metabolism|March 15, 2020
Genetic Architecture Associated With Familial Short StatureYing-Ju Lin, Chi-Fung Cheng, Chung-Hsing Wang, et al.
Scientific Reports|July 27, 2017
Association of human height-related genetic variants with familial short stature in Han Chinese in TaiwanYing-Ju Lin, Wen-Ling Liao, Chung-Hsing Wang, 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.
Pageof 5

Showing results (41-50 of 50) with videos related to

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Pageof 5
You have reached the last page of results.This site can display upto 50 results.
Acta Paediatrica (Oslo, Norway : 1992)|June 1, 2007
Genotype and phenotype in patients with Prader-Willi syndrome in TaiwanHsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang, et al.
Pediatrics and Neonatology|September 12, 2012
A novel 3670-base pair mitochondrial DNA deletion resulting in multi-systemic manifestations in a childHsin-Ming Liu, Li-Ping Tsai, Yin-Hsiu Chien, et al.
American Journal of Medical Genetics. Part A|April 28, 2009
Incidence of the mucopolysaccharidoses in Taiwan, 1984-2004Hsiang-Yu Lin, Shuan-Pei Lin, Chih-Kuang Chuang, et al.
American Journal of Medical Genetics. Part A|April 27, 2018
Functional independence of Taiwanese children with Prader-Willi syndromeChung-Lin Lee, Hsiang-Yu Lin, Li-Ping Tsai, et al.
Journal of the Chinese Medical Association : JCMA|June 24, 2008
Effects of growth hormone treatment on height, weight, and obesity in Taiwanese patients with Prader-Willi syndromeHsiang-Yu Lin, Shuan-Pei Lin, Li-Ping Tsai, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|May 30, 2007
Prader-Willi syndrome in TaiwanHsiang-Yu Lin, Shuan-Pei Lin, Jui-Lung Yen, et al.
The Journal of Clinical Endocrinology and Metabolism|March 15, 2020
Genetic Architecture Associated With Familial Short StatureYing-Ju Lin, Chi-Fung Cheng, Chung-Hsing Wang, et al.
Scientific Reports|July 27, 2017
Association of human height-related genetic variants with familial short stature in Han Chinese in TaiwanYing-Ju Lin, Wen-Ling Liao, Chung-Hsing Wang, 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.
Pageof 5