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Acta Paediatrica (Oslo, Norway : 1992)
|
June 1, 2007
Genotype and phenotype in patients with Prader-Willi syndrome in Taiwan
Hsiang-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 child
Hsin-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, 1984-2004
Hsiang-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 syndrome
Chung-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 syndrome
Hsiang-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 Taiwan
Hsiang-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 Stature
Ying-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 Taiwan
Ying-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 Syndrome
Hsiang-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 Syndrome
Hsiang-Yu Lin, Chung-Lin Lee, Yuan-Rong Tu, et al.
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Showing results (41-50 of 50) with videos related to
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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 Taiwan
Hsiang-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 child
Hsin-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, 1984-2004
Hsiang-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 syndrome
Chung-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 syndrome
Hsiang-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 Taiwan
Hsiang-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 Stature
Ying-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 Taiwan
Ying-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 Syndrome
Hsiang-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 Syndrome
Hsiang-Yu Lin, Chung-Lin Lee, Yuan-Rong Tu, et al.
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of 5