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顯示項目 591331-591355 / 2346275 (共93851頁) << < 23649 23650 23651 23652 23653 23654 23655 23656 23657 23658 > >> 每頁顯示[10|25|50]項目
| 國立交通大學 |
2014-12-08T15:02:04Z |
Molecular conformation and nanomechanics of self-assembled alkylsiloxane monolayers
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Huang, JY; Song, KJ; Lagoutchev, A; Yang, PK; Chuang, TJ |
| 國立交通大學 |
2019-04-02T06:00:51Z |
Molecular conformation and nanomechanics of self-assembled alkylsiloxane monolayers
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Huang, JY; Song, KJ; Lagoutchev, A; Yang, PK; Chuang, TJ |
| 輔英科技大學 |
2009-10-01 |
Molecular connectivity indices for predicting bioactivities of substituted nitrobenzene and aniline compounds
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Lin ,Kuo-Hsiung;Jaw,Ching-Guang ;Yen,Jui-Hung ;Wang,Yei-Shung |
| 臺大學術典藏 |
2018-09-10T07:33:04Z |
Molecular connectivity indices for predicting bioactivities of substituted nitrobenzene and aniline compounds
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Lin, K.-H.;Jaw, C.-G.;Yen, J.-H.;Wang, Y.-S.; Lin, K.-H.; Jaw, C.-G.; Yen, J.-H.; Wang, Y.-S.; JUI-HUNG YEN |
| 國立臺灣大學 |
2009-12 |
Molecular connectivity indices for predicting bioactivities of substituted nitrobenzene and aniline compounds.
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Lin, K.H.; Jaw, C.G.; Yen, J.H.; Wang, Y.S. |
| 臺大學術典藏 |
2022-08-19T06:48:43Z |
Molecular correlates of clinical response and resistance to atezolizumab in combination with bevacizumab in advanced hepatocellular carcinoma
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Wang Y.; Burgoyne A.M.; Dayyani F.; Spahn J.; Verret W.; Finn R.S.; Toh H.C.; Lujambio A.; Yau T.; Kaseb A.O.; Ryoo B.-Y.; He A.R.; CHIH-HUNG HSU; Zhang W.; Koeppen H.; Lu S.; Guan Y.; de Galarreta M.R.; Abbas A.R.; Zhu A.X. |
| 中國醫藥大學 |
2006 |
Molecular cytogenetic analysis of de novo dup(5)(q33.1q31.1) associated with abnormal perinatal findings.
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(Chen CP); (Lin SP,); (Chern SR); 林齊強(Chyi-Chyang Lin); (Li YC,); (Lee CC); 謝麗嬌(Lie-Jiau Hsieh); (Chen WL,); (Wang W) |
| 中國醫藥大學 |
2006 |
Molecular cytogenetic analysis of de novo dup(5)(q35.2q35.3) and review of the literature of pure partial trisomy-5q.
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陳持平(Chen CP,); (Lin SP,); 林齊強(Lin CC,); (Chen YJ,); (Chern SR,); 李月君(Li YC,); 謝麗嬌(Hsieh LJ,); (Lee CC,); (Wang W.) |
| 中國醫藥大學 |
2008-10-19 |
Molecular cytogenetic analysis of small supernumerary marker chromosome from chromosome 22 --- case report
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簡淑錦(Shu-Chin Chien) |
| 亞洲大學 |
2017-04 |
Molecular cytogenetic characterization and prenatal diagnosis of familial Xp22.33 microdeletion encompassing short stature homeobox gene in a male fetus with a favorable outcome
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Wang;;, 陳持平;Chih-Ping Chen;Tsang-Ming K;Tsang-Ming Ko;Liang-Kai Wa;Liang-Kai Wang;Shuan-Pei Li;Shuan-Pei Lin;Schu-Rern Ch;Schu-Rern Chern;Peih-Shan Wu;Peih-Shan Wu;Yen-Ni Chen;Yen-Ni Chen;Shin-Wen Che;Shin-Wen Chen;Meng-Shan Le;Meng-Shan Lee;Wayseen Wang;Wayseen |
| 臺大學術典藏 |
2022-01-15T00:08:30Z |
Molecular cytogenetic characterization of a de novo small supernumerary marker chromosome derived from chromosome 15 in a pregnancy with incidental detection of a maternal Robertsonian translocation of 45,XX,der(13;14) (q10;q10)
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Chen, Chih Ping; MING CHEN; Ma, Gwo Chin; Chang, Shun Ping; Chern, Schu Rern; Chen, Shin Wen; Wu, Fang Tzu; Lee, Meng Shan; Wang, Wayseen |
| 亞洲大學 |
2017-08 |
Molecular cytogenetic characterization of a duplication of 15q24.2-q26.2 associated with anencephaly and neural tube defect
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Wang, 陳持平;Chih-Ping Chen;Chen-Yu Chen;Chen-Yu Chen;Schu-Rern Ch;Schu-Rern Chern;Peih-Shan Wu;Peih-Shan Wu;Shin-Wen Che;Shin-Wen Chen;Shih-Ting La;Shih-Ting Lai;Chen-Chi Lee;Chen-Chi Lee;Chien-Wen Ya;Chien-Wen Yang;Wayseen Wang;Wayseen |
| 亞洲大學 |
2016-10 |
Molecular cytogenetic characterization of an inv dup(15) chromosome presenting as a small supernumerary marker chromosome associated with the inv dup(15) syndrome
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陳持平;Chen, Chih-Ping;*;Li, Shuan-Pei;Lin, Shuan-Pei;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;Town, Dai-Dyi;Town, Dai-Dyi;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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Chen)*, 陳持平(Chih-Ping;Ko), Tsang-Ming K(Tsang-Ming;Huang), Wen-Chu Huan(Wen-Chu;Chern), Schu-Rern Ch(Schu-Rern;Wu), Peih-Shan Wu(Peih-Shan;Chen), Yen-Ni Chen(Yen-Ni;Chen), Shin-Wen Che(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 |
2016-06 |
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;Chih-Ping Chen;*;Tsang-Ming K;Tsang-Ming Ko;Wen-Chu Huan;Wen-Chu Huang;Schu-Rern Ch;Schu-Rern Chern;Peih-Shan Wu;Peih-Shan Wu;Yen-Ni Chen;Yen-Ni Chen;Shin-Wen Che;Shin-Wen Chen;Chen-Chi Lee;Chen-Chi Lee;, ;Chen-Wen Pan,;Wayseen Wang;Wayseen Wang;; |
| 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 |
2017-02 |
Molecular cytogenetic characterization of Jacobsen syndrome ;11q23.3-q25 deletion in a fetus associated with double outlet right ventricle, hypoplastic left heart syndrome and ductus venosus agenesis on prenatal ultrasound
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Wang;;;, 陳持平;Chih-Ping Chen;Liang-Kai Wa;Liang-Kai Wang;Pei-Chen Wu;Pei-Chen Wu;Tung-Yao Cha;Tung-Yao Chang;Schu-Rern Ch;Schu-Rern Chern;Peih-Shan Wu;Peih-Shan Wu;Yen-Ni Chen;Yen-Ni Chen;Shin-Wen Che;Shin-Wen Chen;Wayseen Wang;Wayseen |
| 亞洲大學 |
2017-06 |
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 7 in the male partner of a phenotypically normal couple with repeated spontaneous abortions
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Wang, 陳持平;Chih-Ping Chen;Ming Chen;Ming Chen;Yuh-Ming Hwu;Yuh-Ming Hwu;Shun-Ping Ch;Shun-Ping Chang;Shin-Wen Che;Shin-Wen Chen;Shih-Ting La;Shih-Ting Lai;Chen-Chi Lee;Chen-Chi Lee;Wayseen Wang;Wayseen |
| 臺大學術典藏 |
2018-09-10T18:06:25Z |
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 7 in the male partner of a phenotypically normal couple with repeated spontaneous abortions
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Chen, C.-P. And Chen, M. And Hwu, Y.-M. And Chang, S.-P. And Chen, S.-W. And Lai, S.-T. And Lee, C.-C. And Wang, W.; MING CHEN |
| 亞洲大學 |
2016-12 |
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22->q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder and in
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陳持平;Chen, Chih-Ping;*;Li, Shuan-Pei;Lin, Shuan-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Ya, Chien-Wen;Yang, Chien-Wen;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-12 |
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p11.22→q11.21::) in an 18-year-old female with short stature, obesity, attention deficit hyperactivity disorder, and intellectual disability
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陳持平;Chen, Chih-Ping;*;Li, Shuan-Pei;Lin, Shuan-Pei;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Ya, Chien-Wen;Yang, Chien-Wen;Le, Meng-Shan;Lee, Meng-Shan;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-12 |
Molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from chromosome 8 or r(8)(::p12->q13.1::) associated with phenotypic abnormalities
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陳持平;Chen, Chih-Ping;*;Li, Shuan-Pei;Lin, Shuan-Pei;Lin, Yi-Hui;Lin, Yi-Hui;Ch, Schu-Rern;Chern, Schu-Rern;Wu, Peih-Shan;Wu, Peih-Shan;Chen, Yen-Ni;Chen, Yen-Ni;Che, Shin-Wen;Chen, Shin-Wen;Ya, Chien-Wen;Yang, Chien-Wen;Chen, Wen-Lin;Chen, Wen-Lin;Wang, Wayseen;Wang, Wayseen |
| 亞洲大學 |
2016-10 |
Molecular cytogenetic characterization of Xp22.32->pter deletion and Xq26.3->qter duplication in a male fetus associated with 46,Y,rec(X)dup(Xq)inv(X)(p22.3q26.3), a hypoplastic left heart, short stature and maternal X chromosome pericentric inversion
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陳持平;Chen, Chih-Ping;*;Chen, Chen-Yu;Chen, Chen-Yu;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;Town, Dai-Dyi;Town, Dai-Dyi;Wang, Wayseen;Wang, Wayseen |
| 國立臺灣大學 |
1994 |
Molecular Cytogenetic Studies of Children with marker Chromosomes
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侯家瑋; 劉敬萱; 王作仁; HOU, JIA-WOEI; LIU, CHING-HSUAN; WANG, TSO-REN |
顯示項目 591331-591355 / 2346275 (共93851頁) << < 23649 23650 23651 23652 23653 23654 23655 23656 23657 23658 > >> 每頁顯示[10|25|50]項目
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