| 國立臺灣大學 |
2005-07 |
Chromosomal organization, evolutionary relationship, and expression of zebrafish GnRH family members
|
Kuo, MW; Lou, SW; Postlethwait, J; Chung, BC |
| 東海大學 |
2001 |
Chromosomal polymorphism in the Gray Shrew Crocidura attenuata (Mammalia: Insectivora)
|
Motokawa, M., Harada, M., Wu, Y., Lin, L.-K., Suzuki, H. |
| 臺大學術典藏 |
2021-11-22T02:27:28Z |
Chromosomal polymorphism of ribosomal genes in the genus Oryza
|
Chung, M.-C.; Lee, Y.-I.; Cheng, Y.-Y.; Chou, Y.-J.; Lu, C.-F. |
| 中國醫藥大學 |
2013-04 |
Chromosome 10q Deletion del (10)(q26.1q26.3) is Associated with Cataract
|
張鈺孜(chang, yu-tzu);Chou), 周宜卿(I-Ching;Wang), 王仲興(Chung-Hsing;Chin), 陳震南(Zheng-Nan;Kuo), 郭煌宗(Haung-Tsung;Lin), 林齊強(Chyi-Chyang;Tsai), 蔡長海(Chang-Hai;Tsai)*, 蔡輔仁(Fuu-Jen |
| 亞洲大學 |
2011-09 |
Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization and perinatal findings in a fetus with dup(15)(q26.2q26.3)
|
陳持平;Chen, Chih-Ping;Li-Feng Chen, ;Adam Hwa-Ming Hsieh, ;Wang, Wayseen |
| 中國醫藥大學 |
2011-09 |
Chromosome 15q overgrowth syndrome: prenatal diagnosis, molecular cytogenetic characterization and perinatal findings in a fetus with dup(15)(q26.2q26.3)
|
陳持平(Chih-Ping Chen)*;(Yi-Hui Lin);(Heng-Kien Au);(Chin-Yuan Hsu);(Yu-Peng Liu);(Pei-Chen Wu);(Schu-Rern Chern);(Yu-Ting Chen);(Li-Feng Chen);(Adam Hwa-Ming Hsieh);(Wayseen Wang) |
| 國立交通大學 |
2014-12-08T15:23:14Z |
Chromosome 15q21-22-Related Polymorphisms and Haplotypes Are Associated with Susceptibility to Type-2 Diabetic Nonproliferative Retinopathy
|
Hsieh, Yao-Yuan; Huang, Yu-Chuen; Chang, Chi-Chen; Wang, Yu-Kuo; Lin, Wen-Hsin; Tsai, Fuu-Jen |
| 中國醫藥大學 |
2012-05 |
Chromosome 15q21-22-related polymorphisms and haplotypes are associated with susceptibility to type-2 diabetic nonproliferative retinopathy
|
謝耀元(Hsieh Yao-Yuan);黃毓銓(Yu-Chuen Huang);(Chi-Chen Chang);(Yu-Kuo Wang);林文鑫(Wen-Hsin Lin);蔡輔仁(Fuu-Jen Tsai)* |
| 中國醫藥大學 |
2013-12 |
Chromosome 17p13.3 deletion syndrome: aCGH characterization, prenatal findings and diagnosis, and literature review
|
陳持平(Chih-Ping Chen)*;(Tung-Yao Chang);(Wan-Yuo Guo);(Pei-Chen Wu);(Liang-Kai Wang);(Schu-Rern Chern);(Peih-Shan Wu);蘇俊維(Jun-Wei Su);(Yu-Ting Chen);(Li-Feng Chen);(Wayseen Wang) |
| 亞洲大學 |
201309 |
Chromosome 18p deletion syndrome presenting holoprosencephaly and premaxillary agenesis: prenatal diagnosis and aCGH characterization using uncultured amniocytes
|
陳持平;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Pan, Chen-Wen;Pan, Chen-Wen;Wang, Wayseen;Wang, Wayseen |
| 臺大學術典藏 |
2018-09-10T06:00:32Z |
Chromosome 1p aberrations are frequent in human primary hepatocellular carcinoma
|
Chen, H.-L., Chen, Y.-C., Chen, D.-S.; Hui-Ling Chen; DING-SHINN CHEN |
| 亞洲大學 |
2011-09 |
Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia
|
陳持平;Chen, Chih-Ping |
| 中國醫藥大學 |
2011-09 |
Chromosome 1p32-p31 deletion syndrome: prenatal diagnosis by array comparative genomic hybridization using uncultured amniocytes and association with NFIA haploinsufficiency, ventriculomegaly, corpus callosum hypogenesis, abnormal external genitalia
|
陳持平(Chih-Ping Chen)*;(Yi-Ning Su);(Yi-Yung Chen);(Schu-Rern Chern);(Yu-Peng Liu);(Pei-Chen Wu);(Chen-Chi Lee);(Yu-Ting Chen);(Wayseen Wang) |
| 亞洲大學 |
2010-12 |
Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings
|
陳持平;Chen, Chih-Ping;Chen, Ming;Su, Yi-Ning;Hsu, Chin-Yuan;Tsai, Fuu-Jen;Chern, Schu-Rern;Wu, Pei-Chen;Lee, Chen-Chi;Wang, Wayseen |
| 國立臺灣大學 |
2010 |
Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, Molecular Cytogenetic Characterization and Fetal Ultrasound Findings
|
陳持平; 陳明; 蘇怡寧; 徐金源; 蔡輔仁; 陳樹人; 吳佩臻; 李貞?; CHEN, CHIH-PING; CHEN, MING; SU, YI-NING; HSU, CHIN-YUAN; TSAI, FUU-JEN; CHERN, SCHU-RERN; WU, PEI-CHEN; LEE, CHEN-CHI |
| 中國醫藥大學 |
2010-12 |
Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings
|
陳持平(Chih-Ping Chen)*; (Ming Chen); (Yi-Ning Su); (Chin-Yuan Hsu); 蔡輔仁(Fuu-Jen Tsai); (Schu-Rern Chern); (Pei-Chen Wu); (Chen-Chi Lee); (Wayseen Wang) |
| 國立政治大學 |
2014-11 |
Chromosome 20q13.2 ZNF217 locus amplification correlates with decreased E-cadherin expression in ovarian clear cell carcinoma with PI3K-Akt pathway alterations
|
Huang, H.-N.;Huang, W.-C.;Lin, C.-H.;Huang, Hsin Ying; 黃馨瑩 |
| 國立臺灣大學 |
2014 |
Chromosome 20q13.2 ZNF217 locus amplification correlates with decreased E-cadherin expression in ovarian clear cell carcinoma with PI3K-Akt pathway alterations
|
Huang, Hsien-Neng; Huang, Wen-Chih; Lin, Ching-Hung; Chiang, Ying-Cheng; Huang, Hsin-Ying; Kuo, Kuan-Ting; 林璟宏; 郭冠廷; 江盈澄; 林季宏 |
| 臺大學術典藏 |
2018-09-10T14:52:01Z |
Chromosome 20q13.2 ZNF217 locus amplification correlates with decreased E-cadherin expression in ovarian clear cell carcinoma with PI3K-Akt pathway alterations
|
Huang, Hsien-Neng;Huang, Wen-Chih;Lin, Ching-Hung;Chiang, Ying-Cheng;Huang, Hsin-Ying;Kuo, Kuan-Ting; Huang, Hsien-Neng;Huang, Wen-Chih;Lin, Ching-Hung;Chiang, Ying-Cheng;Huang, Hsin-Ying;Kuo, Kuan-Ting; Huang, H.-N. and Huang, W.-C. and Lin, C.-H. and Chiang, Y.-C. and Huang, H.-Y. and Kuo, K.-T.; 林璟宏;郭冠廷;江盈澄;林季宏; 林璟宏;郭冠廷;江盈澄;林季宏; CHING-HUNG LIN; Huang, Hsien-Neng; Huang, Wen-Chih; KUAN-TING KUO; Lin, Ching-Hung; Chiang, Ying-Cheng; Huang, Hsin-Ying; Kuo, Kuan-Ting |
| 臺大學術典藏 |
2020-02-14T08:50:34Z |
Chromosome 20q13.2 ZNF217 locus amplification correlates with decreased E-cadherin expression in ovarian clear cell carcinoma with PI3K-Akt pathway alterations
|
Huang H.-N; Huang W.-C; Lin C.-H; YING-CHENG CHIANG; Huang H.-Y; Kuo K.-T. |
| 臺大學術典藏 |
2020-03-05T07:52:34Z |
Chromosome 20q13.2 ZNF217 locus amplification correlates with decreased E-cadherin expression in ovarian clear cell carcinoma with PI3K-Akt pathway alterations
|
Huang H.-N.; Huang W.-C.; Lin C.-H.; Chiang Y.-C.; Huang H.-Y.; KUAN-TING KUO |
| 臺大學術典藏 |
2020-03-07T06:42:11Z |
Chromosome 20q13.2 ZNF217 locus amplification correlates with decreased E-cadherin expression in ovarian clear cell carcinoma with PI3K-Akt pathway alterations
|
Huang H.-N.; Huang W.-C.; Lin C.-H.; Chiang Y.-C.; Huang H.-Y.; KUAN-TING KUO |
| 臺大學術典藏 |
2021-02-04T07:44:56Z |
Chromosome 20q13.2 ZNF217 locus amplification correlates with decreased E-cadherin expression in ovarian clear cell carcinoma with PI3K-Akt pathway alterations
|
Huang H.-N.;Huang W.-C.;Lin C.-H.;Ying-Cheng Chiang;Huang H.-Y.;Kuo K.-T.; Huang H.-N.; Huang W.-C.; Lin C.-H.; YING-CHENG CHIANG; Huang H.-Y.; Kuo K.-T. |
| 亞洲大學 |
201309 |
Chromosome 22q11.2 deletion syndrome: prenatal diagnosis, array comparative genomic hybridization characterization using uncultured amniocytes and literature review
|
陳持平;Chen, Chih-Ping;Hua, Jian-Pei;Huang, Jian-Pei;Chen, Yi-Yung;Chen, Yi-Yung;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Su, Jun-Wei;Su, Jun-Wei;Chen, Yu-Ting;Chen, Yu-Ting;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 臺大學術典藏 |
2021-10-25T02:57:32Z |
Chromosome 3p12.3-p14.2 and 3q26.2-q26.32 are genomic markers for prognosis of advanced nasopharyngeal carcinoma
|
Sheu J.J.-C; |Lee C.-H; |JENG-YUH KO; |Tsao G.S.W; |Wu C.-C; |Fang C.-Y; |Tsai F.-J; |Hua C.-H; |Chen C.-L; |Chen J.-Y. |
