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"ko tsang ming"的相关文件
显示项目 1-10 / 121 (共13页)
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| 臺大學術典藏 |
2021-03-02T07:39:46Z |
Massively parallel sequencing analysis of nondegraded and degraded DNA mixtures using the ForenSeq™ system in combination with EuroForMix software
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Hwa, Hsiao-Lin;Ming-Yih Wu;Chung, Wan-Chia;Ko, Tsang-Ming;Lin, Chih-Peng;Yin, Hsiang-I;Lee, Tsui-Ting;Lee, James Chun-I; Hwa, Hsiao-Lin; MING-YIH WU; Chung, Wan-Chia; Ko, Tsang-Ming; Lin, Chih-Peng; Yin, Hsiang-I; Lee, Tsui-Ting; Lee, James Chun-I |
| 亞洲大學 |
2019-11 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 3
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陳持平;Chen, Chih-Ping;Tsang-Ming, K;Ko, Tsang-Ming;Chen, Chen-Yu;Chen, Chen-Yu;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;Wu, Fang-Tzu;Wu, Fang-Tzu;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2019-09 |
Inv dup del(10p): prenatal diagnosis and molecular cytogenetic characterization
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陳持平;Chen, Chih-Ping;Tsang-Ming, K;Ko, Tsang-Ming;Wa, Liang-Kai;Wang, Liang-Kai;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;Wu, Fang-Tzu;Wu, Fang-Tzu;Chen, Li-Feng;Chen, Li-Feng;Wang, Wayseen;Wang, Wayseen |
| 臺大學術典藏 |
2018-09-10T15:39:05Z |
Correlation of IL36RN mutation with different clinical features of pustular psoriasis in Chinese patients
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JIN-BON HONG;?_???;????;???R?z;?????f;???T??;KO, TSANG-MING???N??;SU, YI-NING;TSENG, LI-HUI;CHEN, YA-HUI;LEE, JAMES CHUN-I;HWA, HSIAO-LIN;Tsai, Tsen-Fang;Lin, Sung-Jan;Chan, Chih-Chieh;Hong, Jin-Bong;Chiu, Hsien-Yi;Wang, Ting-Shun;TSEN-FANG TSAI;Tsai, T.-F.;Lin, S.-J.;Chan, C.-C.;Hong, J.-B.;Chiu, H.-Y.;Wang, T.-S.;KO, TSANG-MING;SU, YI-NING;TSENG, LI-HUI;CHEN, YA-HUI;LEE, JAMES CHUN-I;HWA, HSIAO-LIN;Tsai, Tsen-Fang;Lin, Sung-Jan;Chan, Chih-Chieh;Hong, Jin-Bong;Chiu, Hsien-Yi;Wang, Ting-Shun;TSEN-FANG TSAI; Wang, T.-S.; Chiu, H.-Y.; Hong, J.-B.; Chan, C.-C.; Lin, S.-J.; Tsai, T.-F.; Lin, Sung-Jan; Tsai, Tsen-Fang; LEE, JAMES CHUN-I; TSENG, LI-HUI |
| 臺大學術典藏 |
2018-09-10T07:24:55Z |
Thirteen X-chromosomal short tandem repeat loci multiplex data from Taiwanese
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JAMES CHUN-I LEE; HSIAO-LIN HWA; Horng, Yi-shiung; Wu, Ching-yi; Wu, Tai-chieh; Ku, Fang-ling; HWA, HSIAO-LIN; LEE, JAMES CHUN-I; CHEN, YA-HUI; TSENG, LI-HUI; SU, YI-NING; KO, TSANG-MING; Lin, Keh-chung; LI-HUI TSENG; Hsieh, Yu-wei; Hwa, Hsiao-Lin;Lee, James Chun-I;Chen, Ya-Hui;Tseng, Li-Hui;Su, Yi-Ning;Ko, Tsang-Ming;Hwa, Hsiao-Lin;Lee, James Chun-I;Chen, Ya-Hui;Tseng, Li-Hui;Su, Yi-Ning;Ko, Tsang-Ming |
| 國立交通大學 |
2018-08-21T05:53:02Z |
Presymptomatic Diagnosis of Spinal Muscular Atrophy Through Newborn Screening
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Chien, Yin-Hsiu; Chiang, Shu-Chuan; Weng, Wen-Chin; Lee, Ni-Chung; Lin, Ching-Jie; Hsieh, Wu-Shiun; Lee, Wang-Tso; Jong, Yuh-Jyh; Ko, Tsang-Ming; Hwu, Wuh-Liang |
| 亞洲大學 |
2018-02 |
Prenatal diagnosis of short-rib polydactyly syndrome type III or short-rib thoracic dysplasia 3 with or without polydactyly ;SRTD3; associated with compound heterozygous mutations in DYNC2H1 in a fetus
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陳持平;Chen, Chih-Ping;*;Tsang-Ming, K;Ko, Tsang-Ming;Cha, Tung-Yao;Chang, Tung-Yao;Ch, Schu-Rern;Chern, Schu-Rern;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2018-02 |
Prenatal diagnosis of a 0.7-Mb 17p13.3 microdeletion encompassing YWHAE and CRK but not PAFAH1B1 in a fetus without ultrasound abnormalities
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陳持平;Chen, Chih-Ping;*;Tsang-Ming, K;Ko, Tsang-Ming;Wa, Liang-Kai;Wang, Liang-Kai;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Ya, Chien-Wen;Yang, Chien-Wen;Lee, Chen-Chi;Lee, Chen-Chi;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2017-12 |
Prenatal diagnosis and molecular cytogenetic characterization of low-level mosaicism for tetrasomy 18p at amniocentesis in a pregnancy with a favorable outcome
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陳持平;Chen, Chih-Ping;Tsang-Ming, K;Ko, Tsang-Ming;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Che, Shin-Wen;Chen, Shin-Wen;La, Shih-Ting;Lai, Shih-Ting;Chua, Tzu-Yun;Chuang, Tzu-Yun;Ya, Chien-Wen;Yang, Chien-Wen;Pan, Chen-Wen;Wang, Wayseen |
| 亞洲大學 |
2016-10 |
Prenatal diagnosis and molecular cytogenetic characterization of rec(10)dup(10p)inv(10)(p11.2q26.3) in a fetus associated with paternal pericentirc inversion
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陳持平;Chen, Chih-Ping;*;Tsang-Ming, K;Ko, Tsang-Ming;Su, Yi-Ning;Su, Yi-Ning;Wa, Liang-Kai;Wang, Liang-Kai;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Che, Shin-Wen;Town, Dai-Dyi;Town, Dai-Dyi;Chen, Li-Feng;Chen, Li-Feng;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
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