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"chou yen yin"的相關文件
顯示項目 21-31 / 31 (共1頁)
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| 國立成功大學 |
2013-01 |
Factors associated with adolescents' perspectives on health needs and preference for health information sources in Taiwan
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Tsai, Meng-Che; Chou, Yen-Yin; Lin, Shio-Jean; Lin, Sheng-Hsiang |
| 國立成功大學 |
2012-04 |
A novel SRD5A2 mutation in a Taiwanese newborn with ambiguous genitalia
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Tsai, Meng-Che; Chou, Yen-Yin; Lin, Shio-Jean; Tsai, Li-Ping |
| 國立成功大學 |
2012-04 |
Sex-reversed Acampomelic Campomelic Dysplasia With a Homozygous Deletion Mutation in SOX9 Gene
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Chen, Shou-Yen; Lin, Shio-Jean; Tsai, Li-Ping; Chou, Yen-Yin |
| 國立成功大學 |
2011-06 |
Assessment of experience and training needs in adolescent medicine: Perspectives from pediatricians
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Tsai, Meng-Che;Chou, Yen-Yin;Lin, Shio-Jean |
| 國立成功大學 |
2011-05 |
Complex Chromosome Rearrangement 46,XY, der(9)t(Y;9)(q12;p23) in a Girl With Sex Reversal and Mental Retardation
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Lee, I-Wen; Chou, Yen-Yin; Hsu, Keng-Fu; Chou, Pei-Yi; Chen, Ming; Kuo, Pao-Lin; Lin, Shio-Jean |
| 國立成功大學 |
2011-02-20 |
High resolution melting analysis for the detection of SLC25A13 gene mutations in Taiwan
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Lin, Jing-Ting; Hsiao, Kwang-Jen; Chen, Chiung-Yu; Wu, Cheng-Chung; Lin, Shio-Jean; Chou, Yen-Yin; Shiesh, Shu-Chu |
| 國立成功大學 |
2009-01 |
Association between prenatal exposure to phthalates and the health of newborns
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Huang, Po-Chin; Kuo, Pao-Lin; Chou, Yen-Yin; Lin, Shio-Jean; Lee, Ching-Chang |
| 國立成功大學 |
2009-01 |
Phthalate Exposure in Girls During Early Puberty
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Chou, Yen-Yin; Huang, Po-Chin; Lee, Ching-Chang; Wu, Meng-Hsing; Lin, Shio-Jean |
| 國立成功大學 |
2005-07 |
Clinical suppression of precocious puberty with cetrorelix after failed treatment with GnRH agonist in a girl with gonadotrophin-independent precocious puberty
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Wu, Meng-Hsing; Lin, Shio-Jean; Wu, Li-Hsiang; Cheng, Yueh-Chin; Chou, Yen-Yin; Pan, Hsien-An |
| 國立成功大學 |
2005-04 |
A 38.8 kb deletion mutation of the iduronate-2-sulfatase gene in a patient with Hunter syndrome
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Chou, Yen-Yin; Chao, Sheau-Chiou; Kuo, Pan-Lin; Lin, Shio-Jean |
| 國立成功大學 |
2004-10 |
Russell-Silver syndrome: Molecular diagnosis of maternal uniparental disomy of chromosome 7 using methylation, specific polymerase chain reaction assay and single nucleotide polymorphisms genotyping
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Chou, Yen-Yin; Chen, Chien-Chang; Kuo, Pao-Lin; Tsai, Wen-Hui; Lin, Shio-Jean |
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