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Showing items 255711-255720 of 2348685 (234869 Page(s) Totally) << < 25567 25568 25569 25570 25571 25572 25573 25574 25575 25576 > >> View [10|25|50] records per page
| 國立臺灣大學 |
2005 |
Chromosomal Organization, Evolutionary Relationship, and Expression of Zebrafish GnRH Family Members
|
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
|
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) |
Showing items 255711-255720 of 2348685 (234869 Page(s) Totally) << < 25567 25568 25569 25570 25571 25572 25573 25574 25575 25576 > >> View [10|25|50] records per page
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