| 國立臺灣大學 |
2006-07 |
Novel mutation in the TSC2 gene associated with prenatally diagnosed cardiac rhabdomyomas and cerebral tuberous sclerosis
|
Chen, CP; Su, YN; Hung, CC; Shih, JC; Wang, W |
| 臺大學術典藏 |
2021-02-04T06:46:49Z |
Novel mutation in the TSC2 gene associated with prenatally diagnosed cardiac rhabdomyomas and cerebral tuberous sclerosis
|
Chen C.-P.;Su Y.-N.;Hung C.-C.;Jin-Chung Shih;Wang W.; Chen C.-P.; Su Y.-N.; Hung C.-C.; JIN-CHUNG SHIH; Wang W. |
| 國立成功大學 |
2022-09 |
Novel mutation of MAP3K1 gene in 46,XY DSD with complete gonadal dysgenesis
|
Yu;Pei-Hsiu;Tsai;Meng-Che;Chiang;-Ting, Chun;Wang;Han-Yu;Kuo;Pao-Lin |
| 國立臺灣大學 |
2006-07 |
Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal iscemic stroke
|
Tang, SC; Lee, MJ; Jeng, JS; Yip, PK. |
| 國立臺灣大學 |
2006 |
Novel Mutation of Neurofibromatosis Type 1 in a Patient with Cerebral Vasculopathy and Fatal Ischemic Stroke
|
湯頌君; 李銘仁; 鄭建興; 葉炳強; TANG, SUNG-CHUN; LEE, MING-JEN; JENG, JIANN-SHING; YIP, PING-KEUNG |
| 國立臺灣大學 |
2006-06 |
NOVEL MUTATION OF NEUROFIBROMATOSIS TYPE 1 IN A PATIENT WITH CEREBRAL VASCULOPATHY AND FATAL ISCHEMIC STROKE
|
湯頌君; 李銘仁; 鄭建興; 葉炳強 |
| 臺大學術典藏 |
2020-03-04T05:35:24Z |
Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke
|
SUNG-CHUN TANG;Yip P.-K.;Jeng J.-S;Lee M.-J; SUNG-CHUN TANG; Lee M.-J; Jeng J.-S; Yip P.-K. |
| 臺大學術典藏 |
2020-03-02T12:11:30Z |
Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke
|
SUNG-CHUN TANG;Yip P.-K.;Jeng J.-S;Lee M.-J; SUNG-CHUN TANG; Lee M.-J; Jeng J.-S; Yip P.-K. |
| 臺大學術典藏 |
2018-09-10T05:46:48Z |
Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke
|
Tang, S.-C. and Lee, M.-J. and Jeng, J.-S. and Yip, P.-K.; JIANN-SHING JENG; MING-JEN LEE; Sung-Chun Tang |
| 臺大學術典藏 |
2020-03-03T02:33:35Z |
Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke
|
Tang S.-C.; MING-JEN LEE; Jeng J.-S.; Yip P.-K. |
| 臺大學術典藏 |
2020-03-03T03:46:05Z |
Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke
|
Tang S.-C.; Lee M.-J.; JIANN-SHING JENG; Yip P.-K. |
| 臺大學術典藏 |
2020-03-04T05:43:05Z |
Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke
|
SUNG-CHUN TANG; Lee M.-J; Jeng J.-S; Yip P.-K. |
| 臺大學術典藏 |
2006 |
Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke
|
Jeng J.-S.; Yip P.-K.; Lee M.-J.; SUNG-CHUN TANG; Sung-Chun Tang;Lee M.-J.;Jeng J.-S.;Yip P.-K. |
| 臺大學術典藏 |
2006 |
Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke
|
Yip P.-K.; Jeng J.-S.; MING-JEN LEE; Tang S.-C. |
| 臺大學術典藏 |
2006 |
Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke
|
JIANN-SHING JENG; Yip P.-K.; Lee M.-J.; Tang S.-C.; Tang S.-C.;Lee M.-J.;Jiann-Shing Jeng;Yip P.-K. |
| 臺大學術典藏 |
2021-12-22T03:54:38Z |
Novel mutation of neurofibromatosis type 1 in a patient with cerebral vasculopathy and fatal ischemic stroke
|
Tang S.-C.; Lee M.-J.; JIANN-SHING JENG; Yip P.-K. |
| 國家衛生研究院 |
2002-07-01 |
Novel mutation of topoisomerase I in rendering cells resistant to camptothecin
|
Chang, JY; Liu, JF; Juang, SH; Liu, TW; Chen, LT |
| 中國醫藥大學 |
2002-07 |
Novel Mutation of Topoisomerase I in Rendering Cells Resistant to Camptothecin
|
(Chang, J.-Y.*)*; (Liu, J.-F.); 莊聲宏(Shin-Hun Juang); (Liu T.-W.); (Chen, L.-T) |
| 國立臺灣大學 |
1992 |
Novel Mutational Spectrum Induced by Nmethyl-NI-nitro-N-nitrosoguanidine in the Coding Region of the Hyposanthine (Guanine) Phosphoribosyltransferase Gene in Diploid Human Fibroblasts
|
Yang, J. L.; 吳成文; Yang, J. L.; Wu, Cheng-Wen |
| 中山醫學大學 |
2006 |
Novel mutations at carboxyl terminus of CIC-1 channel in myotonia congenita
|
Kuo, H-C;Hsiao, K-M;Chang, L-I;You, T-H;Yeh, T-H;Huang, C-C |
| 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 |
