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Showing items 621956-621965 of 2351427 (235143 Page(s) Totally) << < 62191 62192 62193 62194 62195 62196 62197 62198 62199 62200 > >> View [10|25|50] records per page
| 臺大學術典藏 |
2021-11-30T04:53:13Z |
Novel mutations detection with next-generation sequencing and its association with clinical outcome in unilateral primary aldosteronism
|
Wu C.-H.; Peng K.-Y.; Hwang D.-Y.; Lin Y.-H.; VIN-CENT WU; Chueh J.S. |
| 臺大學術典藏 |
2022-01-03T05:49:19Z |
Novel mutations detection with next-generation sequencing and its association with clinical outcome in unilateral primary aldosteronism
|
Wu C.-H.; Peng K.-Y.; Hwang D.-Y.; Lin Y.-H.; Wu V.-C.; SHIH-CHIEH CHUEH |
| 臺大學術典藏 |
2021-10-21T23:27:13Z |
Novel mutations detection with next-generation sequencing and its association with clinical outcome in unilateral primary aldosteronism
|
Wu, Che Hsiung; Peng, Kang Yung; Hwang, Daw Yang; YEN-HUNG LIN; VIN-CENT WU; Chueh, Jeff S. |
| 國立臺灣師範大學 |
2014-10-27T15:01:12Z |
Novel Mutations in c-Cb1 Ubiquitin Ligase Gene in Taiwanese Lung Cancer
|
譚一泓; Salgia, Ravi; 謝秀梅; 王憶卿 |
| 中山醫學大學 |
2010 |
Novel mutations in the connexin43 (GJA1) and GJA1 pseudogene may contribute to nonsyndromic hearing loss
|
Hui-Mei Hong; Jiann-Jou Yang; Jia-Ching Shieh; Mei-Ling Li; Shuan-Yow Li |
| 國立臺灣大學 |
2001 |
Novel Mutations in the Factor Vii Gene of Taiwanese Factor Vii-Deficient Patients
|
林正修; 林淑華; 楊偉勛; 沈銘鏡; LIN, JEN-SHIOU; LIN, SHU-WHA; YANG, WEI-SHIUNG; SHEN, MING-CHING |
| 國立臺灣大學 |
2001-03 |
Novel mutations in the Factor VII gene of Taiwanese Factor VII-deficient patients
|
Shen, MC; Lin, JS; Lin, SW; Yang, WS; Lin, B. |
| 臺大學術典藏 |
2020-06-22T07:37:18Z |
Novel mutations in the factor VII gene of Taiwanese factor VII-deficient patients
|
Shen M.-C.;Lin J.-S.;Shu-Wha Lin;Yang W.-S.;Lin B.; Shen M.-C.; Lin J.-S.; SHU-WHA LIN; Yang W.-S.; Lin B. |
| 臺大學術典藏 |
2021-05-25T06:36:03Z |
Novel mutations in the factor VII gene of Taiwanese factor VII-deficient patients
|
MING-CHING SHEN; Lin J.-S.; Lin S.-W.; Yang W.-S.; Lin B. |
| 國立成功大學 |
2005-11 |
Novel mutations in the helix termination motif of keratin 3 and keratin 12 in 2 Taiwanese families with Meesmann corneal dystrophy
|
Chen, Ying-Ting; Chao, Sheau-Chiou; Tseng, Sung-Huei |
Showing items 621956-621965 of 2351427 (235143 Page(s) Totally) << < 62191 62192 62193 62194 62195 62196 62197 62198 62199 62200 > >> View [10|25|50] records per page
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