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Showing items 621961-621970 of 2351427 (235143 Page(s) Totally)
<< < 62192 62193 62194 62195 62196 62197 62198 62199 62200 62201 > >>
View [10|25|50] records per page
| 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 |
| 臺大學術典藏 |
2020-12-16T02:25:09Z |
Novel mutations in the mitochondrial complex I assembly gene NDUFAF5 reveal heterogeneous phenotypes
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Abdenur J.E.; Benke P.J.; Taft R.J.; WUH-LIANG HWU; Simon M.T.;Eftekharian S.S.;Stover A.E.;Osborne A.F.;Braffman B.H.;Chang R.C.;Wang R.Y.;Steenari M.R.;Tang S.;Wuh-Liang Hwu;Taft R.J.;Benke P.J.;Abdenur J.E.; Simon M.T.; Eftekharian S.S.; Stover A.E.; Osborne A.F.; Braffman B.H.; Chang R.C.; Wang R.Y.; Steenari M.R.; Tang S. |
| 中山醫學大學 |
2020 |
Novel Mutations in the TMPRSS3 Gene May Contribute to Taiwanese Patients with Nonsyndromic Hearing Loss
|
Wong, SH; Yen, YC; Li, SY; Yang, JJ |
| 國家衛生研究院 |
2003-10 |
Novel mutations involving the NF1 gene coding sequence in neurofibromatosis type 1 patients from Taiwan
|
Liu, MT; Su, JS; Huang, CY; Tsai, SF |
| 國立成功大學 |
2001-03 |
Novel mutations of CYP3A4 in Chinese
|
Hsieh, Kun-Pin; Lin, Yen-Yu; Cheng, Ching-Ling; Lai, Ming-Liang; Lin, Min-Shung; Siest, Jean-Pascal; Huang, Jin-Ding |
| 東海大學 |
2001 |
Novel mutations of SOX10 suggest a dominant negative role in Waardenburg-Shah syndrome.
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Sham M.H., Lui V.C., Chen B.L., Fu M., Tam P.K. |
Showing items 621961-621970 of 2351427 (235143 Page(s) Totally)
<< < 62192 62193 62194 62195 62196 62197 62198 62199 62200 62201 > >>
View [10|25|50] records per page
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