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"ma gwo chin"的相關文件
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| 臺大學術典藏 |
2022-08-09T03:24:28Z |
Preimplantation Genetic Diagnosis in Hereditary Hearing Impairment
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Huang, Wen-Jie; Chiang Yu-ting; Lin, Pei-Hsuan; HSIN-LIN CHEN; Lin, Chi-Fang; Ma, Gwo-Chin; Chang, Shun-Ping; Fan, Jun-Yang; Lin, Shin-Yu; Wu, Chen-Chi; Ming Chen |
| 臺大學術典藏 |
2022-06-17T07:53:24Z |
Preimplantation Genetic Diagnosis in Hereditary Hearing Impairment
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Chen, Hsin-Lin; Lin, Pei-Hsuan; Chiang Yu-ting; Huang, Wen-Jie; Lin, Chi-Fang; Ma, Gwo-Chin; Chang, Shun-Ping; Fan, Jun-Yang; SHIN-YU LIN; Wu, Chen-Chi; MING CHEN |
| 臺大學術典藏 |
2022-06-14T23:24:21Z |
Polyhydramnios as a sole ultrasonographic finding for detecting fetal hemolytic anemia caused by anti-c alloimmunization
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Wang, Shih Chung; Wu, Yun Chia; Wu, Wan Ju; Lee, Mei Hui; Lin, Wen Hsiang; Ma, Gwo Chin; MING CHEN |
| 臺大學術典藏 |
2022-03-14T23:45:39Z |
Prenatal diagnosis and molecular cytogenetic characterization of a familial small supernumerary marker chromosome derived from the acrocentric chromosome 14/22
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Chen, Chih Ping; MING CHEN; Ma, Gwo Chin; Chang, Shun Ping; Chern, Schu Rern; Chen, Shin Wen; Wu, Fang Tzu; Chen, Wen Lin; Lee, Meng Shan; Chen, Yun Yi; Wang, Wayseen |
| 臺大學術典藏 |
2022-01-15T00:08:30Z |
Molecular cytogenetic characterization of a de novo small supernumerary marker chromosome derived from chromosome 15 in a pregnancy with incidental detection of a maternal Robertsonian translocation of 45,XX,der(13;14) (q10;q10)
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Chen, Chih Ping; MING CHEN; Ma, Gwo Chin; Chang, Shun Ping; Chern, Schu Rern; Chen, Shin Wen; Wu, Fang Tzu; Lee, Meng Shan; Wang, Wayseen |
| 臺大學術典藏 |
2022-01-15T00:08:29Z |
Difficulties of Prenatal Genetic Counseling for a Subsequent Child in a Family With Multiple Genetic Variations
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Huang, Ting Xuan; Ma, Gwo Chin; MING CHEN; Li, Wen Fang; Shaw, Steven W. |
| 臺大學術典藏 |
2022-01-15T00:08:21Z |
Preimplantation genetic diagnosis in hereditary hearing impairment
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Chen, Hsin Lin; PEI-HSUAN LIN; Chiang, Yu Ting; Huang, Wen Jie; Lin, Chi Fang; Ma, Gwo Chin; Chang, Shun Ping; Fan, Jun Yang; SHIN-YU LIN; CHEN-CHI WU; MING CHEN |
| 臺大學術典藏 |
2021-09-14T23:19:14Z |
Prenatal diagnosis of true fetal mosaicism with small supernumerary marker chromosome derived from chromosome 16 by funipuncture and molecular cytogenetics including chromosome microarray
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Yao, Tien Yu; Wu, Wan Ju; Law, Kim Seng; Lee, Mei Hui; Chang, Shun Ping; Lee, Dong Jay; Lin, Wen Hsiang; MING CHEN; Ma, Gwo Chin |
| 臺大學術典藏 |
2021-07-15T05:32:33Z |
Comparison of genetic profiling between primary tumor and circulating tumor cells captured by microfluidics in epithelial ovarian cancer: Tumor heterogeneity or Allele dropout?
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Chang, Ting Yu; Chen, Sheng Wen; Lin, Wen Hsiang; Huang, Chung Er; Evans, Mark I.; Chung, I. Fang; Wu, Janne Wha; Ma, Gwo Chin; MING CHEN |
| 臺大學術典藏 |
2021-03-02T03:44:01Z |
Preimplantation Genetic Diagnosis of Neurodegenerative Diseases: Review of Methodologies and Report of Our Experience as a Regional Reference Laboratory
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Liao, Chun-Hua;Chang, Ming-Yuh;Ma, Gwo-Chin;Chang, Shun-Ping;Lin, Chi-Fang;Lin, Wen-Hsiang;Chen, Hsin-Fu;Shee-Uan Chen;Lee, Yi-Chung;Chao, Chi-Chao;Ming Chen;Hsieh, Sung-Tsang; Liao, Chun-Hua; Chang, Ming-Yuh; Ma, Gwo-Chin; Chang, Shun-Ping; Lin, Chi-Fang; Lin, Wen-Hsiang; Chen, Hsin-Fu; SHEE-UAN CHEN; Lee, Yi-Chung; Chao, Chi-Chao; MING CHEN; Hsieh, Sung-Tsang |
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