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显示项目 255381-255405 / 2346275 (共93851页)
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每页显示[10|25|50]项目
| 國家衛生研究院 |
2008-02 |
Chromosomal inversion between rrn operons among Streptococcus mutans serotype c oral and blood isolates
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Huang, WC; Chen, YYM; Teng, LJ; Lien, HT; Chen, JY; Chia, JS |
| 國立臺灣大學 |
2008 |
Chromosomal Inversion between Rrn Operons among Streptococcus Mutans Serotype C Oral and Blood Isolates
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黃紋娟; 鄧麗珍; 陳振陽; 賈景山; HUANG, WEN-CHUAN; TENG, LEE-JENE; CHEN, JEN-YANG; CHIA, JEAN-SAN |
| 臺大學術典藏 |
2018-09-10T06:47:28Z |
Chromosomal inversion between rrn operons among Streptococcus mutans serotype c oral and blood isolates
|
Huang, W.-C. and Chen, Y.-Y.M. and Teng, L.-J. and Lien, H.-T. and Chen, J.-Y. and Chia, J.-S.; 黃紋娟;鄧麗珍;陳振陽;賈景山; Huang, W. C.; Yi-Ywan, M.; Chen-Teng, L. J.; Lien, H. T.; Chen, J. Y.;Chia, J. S.*; HUANG, WEN-CHUAN;TENG, LEE-JENE;CHEN, JEN-YANG;CHIA, JEAN-SAN; LEE-JENE TENG; JEAN-SAN CHIA; HUANG, WEN-CHUAN; TENG, LEE-JENE; CHEN, JEN-YANG; CHIA, JEAN-SAN |
| 臺大學術典藏 |
2020-06-30T06:13:35Z |
Chromosomal inversion between rrn operons among Streptococcus mutans serotype c oral and blood isolates
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Huang W.-C.;Chen Y.-Y.M.;Lee-Jene Teng;Lien H.-T.;Chen J.-Y.;Chia J.-S.; Huang W.-C.; Chen Y.-Y.M.; LEE-JENE TENG; Lien H.-T.; Chen J.-Y.; Chia J.-S. |
| 國立臺灣大學 |
2008-02 |
Chromosomal inversion between rrn operons among Streptococcus mutans serotype c oral and blood isolates.
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Huang, W. C.; Yi-Ywan, M.; Chen-Teng, L. J.; Lien, H. T.; Chen, J. Y.; Chia, J. S.* |
| 國立臺灣大學 |
1998 |
Chromosomal inversion polymorphism in natural populations of Drosophila ruberrima
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Fang, Shu; Lin, Fei-Jann; Chang, Hwei-yu |
| 國立臺灣大學 |
1987 |
Chromosomal Inversions in Drosophila Albomicans in Taiwan
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張慧羽; 林飛棧; Chang, Hwei-Yu; Lin, Fei-Jann |
| 臺大學術典藏 |
2018-09-10T06:34:24Z |
Chromosomal localization and partial genomic structure of the human peroxisome proliferator activated receptor-gamma (hPPARγ) gene
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Beamer, B.A. and Negri, C. and Yen, C.-J. and Gavrilova, O. and Rumberger, J.M. and Durcan, M.J. and Yarnall, D.P. and Hawkins, A.L. and Griffin, C.A. and Burns, D.K. and Roth, J. and Reitman, M. and Shuldiner, A.R.; CHUNG-JEN YEN |
| 臺大學術典藏 |
1997 |
Chromosomal localization and partial genomic structure of the human peroxisome proliferator activated receptor-gamma (hPPARγ) gene
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Burns D.K.; Griffin C.A.; Hawkins A.L.; Yarnall D.P.; Rumberger J.M.; Durcan M.J.; Gavrilova O.; CHUNG-JEN YEN; Negri C.; Beamer B.A.; Roth J.; Reitman M.; Shuldiner A.R. |
| 國立臺灣大學 |
2005 |
Chromosomal Organization, Evolutionary Relationship, and Expression of Zebrafish GnRH Family Members
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Kuo, Ming-Wei; Lou, Show-Wan; Postlethwait, John; Chung, Bon-Chu |
| 國立臺灣大學 |
2005-07 |
Chromosomal organization, evolutionary relationship, and expression of zebrafish GnRH family members
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Kuo, MW; Lou, SW; Postlethwait, J; Chung, BC |
| 東海大學 |
2001 |
Chromosomal polymorphism in the Gray Shrew Crocidura attenuata (Mammalia: Insectivora)
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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
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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
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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)
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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)
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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
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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
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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
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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
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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
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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
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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
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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
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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 |
| 中國醫藥大學 |
2010-12 |
Chromosome 1p36 deletion syndrome: prenatal diagnosis, molecular cytogenetic characterization and fetal ultrasound findings
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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) |
显示项目 255381-255405 / 2346275 (共93851页)
<< < 10211 10212 10213 10214 10215 10216 10217 10218 10219 10220 > >>
每页显示[10|25|50]项目
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