Suchergebnisse - Chao, Mei‐Chyn
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Growth Hormone Deficiency in a Case of Crouzon Syndrome with Hydrocephalus von Wen, Mei-Hong, Hsiao, Hui-Pin, Chao, Mei-Chyn, Tsai, Fuu-Jen
Veröffentlicht 2010Text -
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CYP17A1 Intron Mutation Causing Cryptic Splicing in 17α-Hydroxylase Deficiency von 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
Veröffentlicht 2011Text -
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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 von 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.
Veröffentlicht 2013Text -
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CD40 Gene Polymorphisms Associated with Susceptibility and Coronary Artery Lesions of Kawasaki Disease in the Taiwanese Population von 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
Veröffentlicht 2012Text -
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Mutations in Pseudohypoparathyroidism 1a and Pseudopseudohypoparathyroidism in Ethnic Chinese von 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
Veröffentlicht 2014Text -
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Survival and diagnostic age of 175 Taiwanese patients with mucopolysaccharidoses (1985–2019) von 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
Veröffentlicht 2020Text -
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Functional independence of Taiwanese patients with mucopolysaccharidoses von 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
Veröffentlicht 2019Text -
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Epigenotype, Genotype, and Phenotype Analysis of Taiwanese Patients with Silver–Russell Syndrome von 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
Veröffentlicht 2021Text