Результати пошуку - Chao, Mei-Chyn
- Показ 1 - 14 результатів із 14
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Growth Hormone Deficiency in a Case of Crouzon Syndrome with Hydrocephalus за авторством Wen, Mei-Hong, Hsiao, Hui-Pin, Chao, Mei-Chyn, Tsai, Fuu-Jen
Опубліковано 2010Текст -
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Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese за авторством Lim, Lee-Moay, Zhao, Xuan, Chao, Mei-Chyn, Chang, Jer-Ming, Chang, Wei-Chiao, Kao, Hung-Ying, Hwang, Daw-Yang, Chen, Hung-Chun
Опубліковано 2015Текст -
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Low penetrance of retinoblastoma for p.V654L mutation of the RB1 gene за авторством Hung, Chia-Cheng, Lin, Shin-Yu, Lee, Chien-Nan, Chen, Chih-Ping, Lin, Shuan-Pei, Chao, Mei-Chyn, Chiou, Shyh-Shin, Su, Yi-Ning
Опубліковано 2011Текст -
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Altered Pattern of Macrophage Polarization as a Biomarker for Severity of Childhood Asthma за авторством Kuo, Chang-Hung, Tsai, Mei-Lan, Li, Chung-Hsiang, Hsiao, Hui-Pin, Chao, Mei-Chyn, Lee, Ming-Sheng, Lin, Yi-Ching, Hung, Chih-Hsing
Опубліковано 2021Текст -
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Intake of Phthalate-Tainted Foods Alters Thyroid Functions in Taiwanese Children за авторством Wu, Ming-Tsang, Wu, Chia-Fang, Chen, Bai-Hsiun, Chen, Eric K., Chen, Yi-Ling, Shiea, Jentaie, Lee, Wei-Te, Chao, Mei-Chyn, Wu, Jiunn-Ren
Опубліковано 2013Текст -
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Fatty Acid Oxidation Disorders in a Chinese Population in Taiwan за авторством Chien, Yin-Hsiu, Lee, Ni-Chung, Chao, Mei-Chyn, Chen, Li-Chu, Chen, Li-Hsin, Chien, Chun-Ching, Ho, Hui-Chen, Suen, Jeng-Hung, Hwu, Wuh-Liang
Опубліковано 2013Текст -
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CYP17A1 Intron Mutation Causing Cryptic Splicing in 17α-Hydroxylase Deficiency за авторством Hwang, Daw-Yang, Hung, Chi-Chih, Riepe, Felix G., Auchus, Richard J., Kulle, Alexandra E., Holterhus, Paul-Martin, Chao, Mei-Chyn, Kuo, Mei-Chuan, Hwang, Shang-Jyh, Chen, Hung-Chun
Опубліковано 2011Текст -
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Novel B3GALTL mutations in classic Peters Plus syndrome and lack of mutations in a large cohort of patients with similar phenotypes за авторством Weh, Eric, Reis, Linda M., Tyler, Rebecca C., Bick, David, Rhead, William J., Wallace, Stephanie, McGregor, Tracy L., Dills, Shelley K., Chao, Mei-Chyn, Murray, Jeffrey C., Semina, Elena V.
Опубліковано 2013Текст -
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CD40 Gene Polymorphisms Associated with Susceptibility and Coronary Artery Lesions of Kawasaki Disease in the Taiwanese Population за авторством Kuo, Ho-Chang, Chao, Mei-Chyn, Hsu, Yu-Wen, Lin, Ying-Chi, Huang, Ying-Hsien, Yu, Hong-Ren, Hou, Ming-Feng, Liang, Chi-Di, Yang, Kuender D., Chang, Wei-Chiao, Wang, Chih-Lu
Опубліковано 2012Текст -
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Mutations in Pseudohypoparathyroidism 1a and Pseudopseudohypoparathyroidism in Ethnic Chinese за авторством Wu, Yi-Lei, Hwang, Daw-Yang, Hsiao, Hui-Pin, Ting, Wei-Hsin, Huang, Chi-Yu, Tsai, Wen-Yu, Chen, Hung-Chun, Chao, Mei-Chyn, Lo, Fu-Sung, Tsai, Jeng-Daw, Yang, Stone, Shih, Shin-Lin, Lin, Shuan-Pei, Lin, Chiung-Ling, Lee, Yann-Jinn
Опубліковано 2014Текст -
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Survival and diagnostic age of 175 Taiwanese patients with mucopolysaccharidoses (1985–2019) за авторством Lin, Hsiang-Yu, Lee, Chung-Lin, Chang, Chia-Ying, Chiu, Pao Chin, Chien, Yin-Hsiu, Niu, Dau-Ming, Tsai, Fuu-Jen, Hwu, Wuh-Liang, Lin, Shio Jean, Lin, Ju-Li, Chao, Mei-Chyn, Chang, Tung-Ming, Tsai, Wen-Hui, Wang, Tzu-Jou, Chuang, Chih-Kuang, Lin, Shuan-Pei
Опубліковано 2020Текст -
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Functional independence of Taiwanese patients with mucopolysaccharidoses за авторством Lee, Chung‐Lin, Lin, Hsiang‐Yu, Chuang, Chih‐Kuang, Chiu, Huei‐Ching, Tu, Ru‐Yi, Huang, You‐Hsin, Hwu, Wuh‐Liang, Tsai, Fuu‐Jen, Chiu, Pao‐Chin, Niu, Dau‐Ming, Chen, Yann‐Jang, Chao, Mei‐Chyn, Chang, Tung‐Ming, Lin, Ju‐Li, Chang, Chia‐Ying, Kao, Yu‐Chia, Lin, Shuan‐Pei
Опубліковано 2019Текст -
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Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver–Russell Syndrome за авторством Lin, Hsiang-Yu, Lee, Chung-Lin, Fran, Sisca, Tu, Ru-Yi, Chang, Ya-Hui, Niu, Dau-Ming, Chang, Chia-Ying, Chiu, Pao-Chin, Chou, Yen-Yin, Hsiao, Hui-Pin, Tsai, Meng-Che, Chao, Mei-Chyn, Tsai, Li-Ping, Yang, Chia-Feng, Su, Pen-Hua, Pan, Yu-Wen, Lee, Chen-Hao, Chu, Tzu-Hung, Chuang, Chih-Kuang, Lin, Shuan-Pei
Опубліковано 2021Текст