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"ko tsang ming"
Showing items 1-50 of 121 (3 Page(s) Totally)
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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 |
| 亞洲大學 |
2016-06 |
Molecular cytogenetic characterization of inv dup del;8p; in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction
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陳持平;Chen, Chih-Ping;*;Tsang-Ming, K;Ko, Tsang-Ming;Huan, Wen-Chu;Huang, Wen-Chu;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Lee, Chen-Chi;Lee, Chen-Chi;Chen-Wen Pan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-06 |
Molecular cytogenetic characterization of inv dup del(8p) in a fetus associated with ventriculomegaly, hypoplastic left heart, polyhydramnios and intestinal obstruction
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陳持平;Chen, Chih-Ping;*;Tsang-Ming, K;Ko, Tsang-Ming;Huan, Wen-Chu;Huang, Wen-Chu;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Lee, Chen-Chi;Lee, Chen-Chi;Chen-Wen Pan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-04 |
Prenatal diagnosis of low-level mosaicism for trisomy 2 associated with a favorable pregnancy outcome
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陳持平;Chen, Chih-Ping;*;Tsang-Ming, K;Ko, Tsang-Ming;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Chen, Li-Feng;Chen, Li-Feng;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-02 |
Prenatal diagnosis of 22q11.2 deletion syndrome associated with right aortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion
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Chen, Yen-Ni;Chen, Yen-Ni;陳持平*;Tsang-Ming, K;Ko, Tsang-Ming;Wa, Liang-Kai;Wang, Liang-Kai;Wu, Pei-Chen;Wu, Pei-Chen;Cha, Tung-Yao;Chang, Tung-Yao;Wu, Peih-Shan;Wu, Peih-Shan;Ya, Chien-Wen;Yang, Chien-Wen;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201502 |
Detection of de novo secondary trisomy 13 due to isochromosome ;13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma
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陳持平*; Tsang-Ming, K;Ko, Tsang-Ming;Hu, Ming-Chao;Huang, Ming-Chao;Ch, Schu-Rern;Chern, Schu-Rern;Lin, Tan-Wei;Lin, Tan-Wei;Cha, Tung-Yao;Chang, Tung-Yao;Kuo, Yu-Ling;Kuo, Yu-Ling;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2015-02 |
Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q) of paternal origin in a pregnancy with fetal cystic hygroma
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陳持平*;Tsang-Ming, K;Ko, Tsang-Ming;Hu, Ming-Chao;Huang, Ming-Chao;Ch, Schu-Rern;Chern, Schu-Rern;Lin, Tan-Wei;Lin, Tan-Wei;Cha, Tung-Yao;Chang, Tung-Yao;Kuo, Yu-Ling;Kuo, Yu-Ling;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2015-02 |
Detection of de novo secondary trisomy 13 due to isochromosome ;13q;13q; of paternal origin in a pregnancy with fetal cystic hygroma
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陳持平;Tsang-Ming, K;Ko, Tsang-Ming;Hu, Ming-Chao;Huang, Ming-Chao;Ch, Schu-Rern;Chern, Schu-Rern;Lin, Tan-Wei;Lin, Tan-Wei;Cha, Tung-Yao;Chang, Tung-Yao;Kuo, Yu-Ling;Kuo, Yu-Ling;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2015-02 |
Detection of de novo secondary trisomy 13 due to isochromosome (13q;13q ; of paternal origin in a pregnancy with fetal cystic hygroma
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;Ko, Tsang-Ming;Hu, Ming-Chao;Huang, Ming-Chao;Ch, Schu-Rern;Chern, Schu-Rern;Lin, Tan-Wei;Lin, Tan-Wei;Cha, Tung-Yao;Chang, Tung-Yao;Kuo, Yu-Ling;Kuo, Yu-Ling;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2014-03 |
Interphase FISH on uncultured amniocytes at repeat amniocentesis for rapid confirmation of low-level mosaicism for tetrasomy 18p
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陳持平;Chen, Chih-Ping;Lin, Chen-Ju;Lin, Chen-Ju;Tsang-Ming, K;Ko, Tsang-Ming;Ch, Schu-Rern;Chern, Schu-Rern;Chen, Yu-Ting;Chen, Yu-Ting;Wu, Peih-Shan;Wu, Peih-Shan;Kuo, Yu-Ling;Kuo, Yu-Ling;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
201309 |
Mosaic trisomy 14 at amniocentesis: prenatal diagnosis and literature review
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陳持平;Chen, Chih-Ping;Wang, Kuo-Gon;Wang, Kuo-Gon;Tsang-Ming, K;Ko, Tsang-Ming;Ch, Schu-Rern;Chern, Schu-Rern;Su, Jun-Wei;Su, Jun-Wei;Town, Dai-Dyi;Town, Dai-Dyi;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2013-09 |
Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 22 associated with cat eye syndrome
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陳持平;Chen, Chih-Ping;Tsang-Ming, K;Ko, Tsang-Ming;Chen, Yi-Yung;Su, Jun-Wei;Wang, Wayseen; |
| 亞洲大學 |
2013-01 |
Array comparative genomic hybridization characterization of prenatally detected de novo apparently balanced reciprocal translocations with or without genomic imbalance in other chromosome
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陳持平;Chen, Chih-Ping;Chen, Ming;Chen, Ming;Ma, Gwo-Chin;Ma, Gwo-Chin;Su, Yi-Ning;Su, Yi-Ning;Tsang-Ming, K;Ko, Tsang-Ming;Lin, Yi-Hui;Lin, Yi-Hui;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2010-12 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 8
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陳持平;Chen, Chih-Ping;Chen, Ming;Ko, Tsang-Ming;Ma, Gwo-Chin;Tsai, Fuu-Jen;Tsai, Ming-Song;Wu, Pei-Chen;Lee, Chen-Chi;Che, Li-Feng;Wang, Wayseen |
| 亞洲大學 |
2010-09 |
Prenatal diagnosis and molecular cytogenetic characterization of a small supernumerary marker chromosome derived from chromosome 21
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陳持平;Chen, Chih-Ping;Lin, Chyi-Chyang;Ko, Tsang-Ming;Tsai, Fuu-Jen;Chern, Schu-Rern;Lee, Chen-Chi;Chen, Yu-Ting;Wu, Pei-Chen;Wang, Wayseen |
| 國立臺灣大學 |
2009 |
Thirteen X-Chromosomal Short Tandem Repeat Loci Multiplex Data from Taiwanese
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華筱玲; 李俊億; 陳雅惠; 曾麗慧; 蘇怡寧; 柯滄銘; HWA, HSIAO-LIN; LEE, JAMES CHUN-I; CHEN, YA-HUI; TSENG, LI-HUI; SU, YI-NING; KO, TSANG-MING |
| 國立臺灣大學 |
2009 |
Pseudogene-Derived Ikbkg Gene Mutations in Incontinentia Pigmenti
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李妮鍾; 胡務亮; 簡穎秀; 柯滄銘; LEE, NI-CHUNG; HWU, WUH-LIANG; CHIEN, YIN-HSIU; KO, TSANG-MING |
| 國立臺灣大學 |
2007 |
The Carrier Frequency and Mutation Profile Of? Eta-Thalassemia in Taiwan
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林凱信; 張淑惠; 蘇怡寧; 蘇喜; 柯滄銘; LIN, KAI-HSIN; CHANG, SHU-HUI; SU, YI- NING; SU, SYI; KO, TSANG-MING |
| 國立臺灣大學 |
2007 |
Risk Prediction for Down's Syndrome in Young Pregnant Women Using Maternal Serum Biomarkers: Determination of Cut-Off Risk from Receiver Operating Characteristic Curve Analysis
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華筱玲; 柯滄銘; 謝豐舟; 嚴明芳; 周楷沛; 陳秀熙; HWA, HSIAO-LIN; KO, TSANG-MING; HSIEH, FON-JOU; YEN, AMY MING-FANG; CHOU, KAI-PEI; CHEN, TONY HSIU-HSI |
| 國立臺灣大學 |
2007 |
Multiplex Ligation-Dependent Probe Amplification Identification of Deletions and Duplications of the Duchenne Muscular Dystrophy Gene in Taiwanese Subjects
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華筱玲; 陳春雄; 鐘育志; 趙美琴; 柯滄銘; HWA, HSIAO-LIN; CHEN, CHUNG-HSIUNG; JONG, YUH-JYH; CHAO, MEI-CHYN; KO, TSANG-MING |
| 國立臺灣大學 |
2006 |
Prenatal Diagnosis and Genetic Analysis of a Fetus with 47,Xx,+21/46,Xx Mosaicism and Xx/Xy Chimerism
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華筱玲; 柯滄銘; 張麗束; HWA, HSIAO-LIN; KO, TSANG-MING; CHANG, LI-SHU |
| 國立臺灣大學 |
2004 |
Fetal Gender Determination Using Real-Time Quantitative Polymerase Chain Reaction Analysis of Maternal Plasma
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華筱玲; 柯滄銘; 嚴孟祿; 江郁霖; HWA, HSIAO-LIN; KO, TSANG-MING; YEN, MENG-LUH; CHIANG, YU-LING |
| 國立臺灣大學 |
2004 |
Prenatal Diagnosis of Mos46,X,Del(Y)(Q11.2)/45,X by Cytogenetic and Molecular Studies with Multiplex Str Analysis
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華筱玲; 柯滄銘; 蘇怡寧; 曾麗慧; 謝豐舟; HWA, HSIAO-LIN; KO, TSANG-MING; SU, YI-NING; TSENG, LI-HUI; HSIEH, FON-JOU |
| 國立臺灣大學 |
2004 |
Evaluation of Second Trimester Maternal Serum Screening for Down's Syndrome Using the Spiegelhalter-Knill-Jones (S-Kj) Approach
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華筱玲; 嚴孟祿; 謝豐舟; 柯滄銘; 陳秀熙; HWA, HSIAO-LIN; YEN, MENG-LUH; HSIEH, FON-JOU; KO, TSANG-MING; CHEN, TONY HSIU-HIS |
| 國立臺灣大學 |
2003 |
Mutation Spectrum of the Connexin 26 (Gjb2) Gene in Taiwanese Patients with Prelingual Deafness
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華筱玲; 柯滄銘; 許權振; HWA, HSIAO-LIN; KO, TSANG-MING; HSU, CHUAN-JEN |
| 國立臺灣大學 |
1999 |
Molecular Characterization of the – Fil Determinant of Alpha-Thalassemia
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柯滄銘; KO, TSANG-MING |
| 國立臺灣大學 |
1999 |
The Deletion of a Thymidine at Codon 228 of Coagulation Factor 9 Causes Hemophilia B in a Taiwanese Patient
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柯滄銘; KO, TSANG-MING |
| 國立臺灣大學 |
1999 |
Homozygous 341delg/101x of Gulcose-6-Phosphatase(G6pt) Gene Causes Glycogen Storage Disease Type Ia (Von Gierke Disease) in a Chinese Patient
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柯滄銘; 胡務亮; KO, TSANG-MING; HWU, WUH-LIANG |
| 國立臺灣大學 |
1999 |
Molecular Genetic Study of Pompe Disease in Chinese Patients in Taiwan
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柯滄銘; 胡務亮; 林玉婉; 曾麗慧; 華筱玲; 王作仁; 莊壽洺; KO, TSANG-MING; HWU, WUH-LIANG; LIN, YU-WAN; TSENG, LI-HUI; HWA, HSIAO-LIN; WANG, TSO-REN; CHUANG, SOU-MING |
| 國立臺灣大學 |
1998 |
Second-Trimester Genetic Amniocentesis in Twin Pregnancy
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柯滄銘; 曾麗慧; 華筱玲; KO, TSANG-MING; TSENG, LI-HUI; HWA, HSIAO-LIN |
| 國立臺灣大學 |
1998 |
Congenital Adrenal Hyperplasia- Molecular Characterization
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柯滄銘; 曾麗慧; 華筱玲; 徐碧梅; 莊壽洺; 李鎡堯; KO, TSANG-MING; TSENG, LI-HUI; HWA, HSIAO-LIN; HSU, PI-MEI; CHUANG, SOU-MING; LEE, TZU-YAO |
| 國立臺灣大學 |
1998 |
Molecular Characterization and Pcr Diagnosis of Thailand Deletion of Alpha-Globin Gene Cluster
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柯滄銘; 曾麗慧; 華筱玲; 徐碧梅; 黎淑芳; 莊壽洺; KO, TSANG-MING; TSENG, LI-HUI; HWA, HSIAO-LIN; HSU, PI-MEI; LI, SHU-FUNG; CHUANG, SOU-MING |
| 國立臺灣大學 |
1998 |
Fluorescence Microsatellite Analysis to Study the Parental Origin of the Supernumerary Chromosome in Down's Syndrome
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柯滄銘; 華筱玲; 曾麗慧; KO, TSANG-MING; HWA, HSIAO-LIN; TSENG, LI-HUI |
| 國立臺灣大學 |
1997 |
Molecular Characterization of Beta-Thalassemia in Taiwan and the Identification of Two New Mutations
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柯滄銘; 曾麗慧; 徐碧梅; 黎淑芳; 莊壽洺; KO, TSANG-MING; TSENG, LI-HUI; HSU, PI-MEI; LI, SHU -FUNG; CHUANG, SOU-MING |
| 國立臺灣大學 |
1997 |
Misdiagnosis of Homozygous Alpha-Thalassaemia 1 May Occur If Polymerase Chain Reaction Alone Is Used in Prenatal Diagnosis
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柯滄銘; 曾麗慧; 華筱玲; 徐碧梅; 黎淑芳; 朱若愚; 呂佩貞; 李鎡堯; 莊壽洺; KO, TSANG-MING; TSENG, LI-HUI; HWA, HSIAO-LIN; HSU, PI-MEI; LI, SHU-FUNG; CHU, JO-YU; LU, PEI-JEN; LEE, TZU-YAO; CHUANG, SOU-MING |
| 國立臺灣大學 |
1996 |
子宮肌瘤的核型分析
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柯滄銘; 李鎡堯; 莊壽洺; Ko, Tsang-Ming; Lee, Tzu-Yao; Chuang, Sou-Ming |
| 國立臺灣大學 |
1995 |
Recurrent Down Syndrome Due to Trisomy 21 Mosaicism in the Ovary
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Tseng, Li-Hui; 莊壽洺; Lee, Tzu-Yao; 柯滄銘; Tseng, Li-Hui; Chuang, Sou-Ming; Lee, Tzu-Yao; Ko, Tsang-Ming |
| 國立臺灣大學 |
1995 |
Ultrasonographic Scanning of Placental Thickness and the Prenatal Diagnosis of Homozygous Alpha-thalassemia 1 in the Second Trimester
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柯滄銘; Tseng, Li-Hui; Lee, Tzu-Yao; 莊壽洺; Ko, Tsang-Ming; Tseng, Li-Hui; Lee, Tzu-Yao; Chuang, Sou-Ming |
| 國立臺灣大學 |
1994-04 |
以核酸聚合??連鎖反應進行東南亞型甲型海洋性貧血的帶因者檢查和產前診斷
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柯滄銘; Ko, Tsang-Ming |
| 國立臺灣大學 |
1994-03 |
Infrequent Mutation in Tumor Suppressor Gene P53 in Gestational Trophoblastic Neoplasia
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Chen, Chi-An; 陳燕惠; 陳擇銘; Ko, Tsang-Ming; Wu, Chih-Cheng; Lee, Chien-Nan; 謝長堯; Chen, Chi-An; 陳燕惠; 陳擇銘; Ko, Tsang-Ming; Wu, Chih-Cheng; Lee, Chien-Nan; Hsieh, Chang-Yao |
| 國立臺灣大學 |
1994 |
Prevalence and Molecular Studies of Thalassemia in Five Aboriginal Groups in Taiwan
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柯滄銘; 曾麗慧; 鄭泰安; 華筱玲; 張幼國; 莊壽洺; 李鎡堯; KO, TSANG-MING; TSENG, LI-HUI; CHENG, ANDREW, TAI-ANN; HWA, HSIAO-LIN; CHANG, YUO-KUO; CHUANG, SOU-MING; LEE, TZU-YAO |
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