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Taiwan Academic Institutional Repository >
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"柯滄銘"
Showing items 1-10 of 120 (12 Page(s) Totally) 1 2 3 4 5 6 7 8 9 10 > >> View [10|25|50] records per page
| 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 |
Showing items 1-10 of 120 (12 Page(s) Totally) 1 2 3 4 5 6 7 8 9 10 > >> View [10|25|50] records per page
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