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Mei-Chyn Chao

Showing results (41-50 of 65) with videos related to

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Molecular Genetics and Metabolism|November 28, 2007
Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiencyHsien-Hsiung Lee, Yann-Jinn Lee, Yu-Mei Wang, et al.
JIMD Reports|May 24, 2013
Fatty Acid oxidation disorders in a chinese population in taiwanYin-Hsiu Chien, Ni-Chung Lee, Mei-Chyn Chao, et al.
American Journal of Medical Genetics. Part A|January 8, 2005
Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotypeChing-Cherng Tzeng, Li-Ping Tsai, Wuh-Liang Hwu, et al.
The Kaohsiung Journal of Medical Sciences|September 15, 2010
Ganglioneuroma of posterior mediastinum in a 6-year-old girl: imaging for pediatric intrathoracic incidentalomaPei-Chin Lin, Shih-Hsiung Lin, Shah-Hwa Chou, et al.
International Journal of Hematology|December 24, 2004
Case of chronic lymphocytic leukemia with unusual chromosome aberrationsHui-Hua Hsiao, Yi-Hui Hung, Hui-Pin Hsiao, et al.
Plos One|October 4, 2011
CYP17A1 intron mutation causing cryptic splicing in 17α-hydroxylase deficiencyDaw-Yang Hwang, Chi-Chih Hung, Felix G Riepe, et al.
Blood Cells, Molecules & Diseases|July 3, 2014
Outcome of early-treated type III Gaucher disease patientsNi-Chung Lee, Yin-Hsiu Chien, Siew-Lee Wong, et al.
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.
Thescientificworldjournal|May 31, 2012
CD40 Gene polymorphisms associated with susceptibility and coronary artery lesions of Kawasaki disease in the Taiwanese populationHo-Chang Kuo, Mei-Chyn Chao, Yu-Wen Hsu, et al.
Molecular Genetics and Metabolism|May 25, 2016
3-O-methyldopa levels in newborns: Result of newborn screening for aromatic l-amino-acid decarboxylase deficiencyYin-Hsiu Chien, Pin-Wen Chen, Ni-Chung Lee, et al.
Pageof 7

Showing results (41-50 of 65) with videos related to

Sort By:
Pageof 7
Molecular Genetics and Metabolism|November 28, 2007
Low frequency of the CYP21A2 deletion in ethnic Chinese (Taiwanese) patients with 21-hydroxylase deficiencyHsien-Hsiung Lee, Yann-Jinn Lee, Yu-Mei Wang, et al.
JIMD Reports|May 24, 2013
Fatty Acid oxidation disorders in a chinese population in taiwanYin-Hsiu Chien, Ni-Chung Lee, Mei-Chyn Chao, et al.
American Journal of Medical Genetics. Part A|January 8, 2005
Prevalence of the FMR1 mutation in Taiwan assessed by large-scale screening of newborn boys and analysis of DXS548-FRAXAC1 haplotypeChing-Cherng Tzeng, Li-Ping Tsai, Wuh-Liang Hwu, et al.
The Kaohsiung Journal of Medical Sciences|September 15, 2010
Ganglioneuroma of posterior mediastinum in a 6-year-old girl: imaging for pediatric intrathoracic incidentalomaPei-Chin Lin, Shih-Hsiung Lin, Shah-Hwa Chou, et al.
International Journal of Hematology|December 24, 2004
Case of chronic lymphocytic leukemia with unusual chromosome aberrationsHui-Hua Hsiao, Yi-Hui Hung, Hui-Pin Hsiao, et al.
Plos One|October 4, 2011
CYP17A1 intron mutation causing cryptic splicing in 17α-hydroxylase deficiencyDaw-Yang Hwang, Chi-Chih Hung, Felix G Riepe, et al.
Blood Cells, Molecules & Diseases|July 3, 2014
Outcome of early-treated type III Gaucher disease patientsNi-Chung Lee, Yin-Hsiu Chien, Siew-Lee Wong, et al.
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.
Thescientificworldjournal|May 31, 2012
CD40 Gene polymorphisms associated with susceptibility and coronary artery lesions of Kawasaki disease in the Taiwanese populationHo-Chang Kuo, Mei-Chyn Chao, Yu-Wen Hsu, et al.
Molecular Genetics and Metabolism|May 25, 2016
3-O-methyldopa levels in newborns: Result of newborn screening for aromatic l-amino-acid decarboxylase deficiencyYin-Hsiu Chien, Pin-Wen Chen, Ni-Chung Lee, et al.
Pageof 7