English  |  正體中文  |  简体中文  |  Total items :0  
Visitors :  52707145    Online Users :  615
Project Commissioned by the Ministry of Education
Project Executed by National Taiwan University Library
 
臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)
About TAIR

Browse By

News

Copyright

Related Links

"hsu c j"

Return to Browse by Author
Sorting by Title Sort by Date

Showing items 101-110 of 419  (42 Page(s) Totally)
<< < 6 7 8 9 10 11 12 13 14 15 > >>
View [10|25|50] records per page

Institution Date Title Author
臺大學術典藏 2021-08-05T02:41:21Z A novel synthesis of sulfurized magnetic biochar for aqueous Hg(II) capture as a potential method for environmental remediation in water Hsu C.-J;Cheng Y.-H;Huang Y.-P;Atkinson J.D;Hsi H.-C.; Hsu C.-J; Cheng Y.-H; Huang Y.-P; Atkinson J.D; Hsi H.-C.; HSING-CHENG HSI
臺大學術典藏 2021-08-05T02:41:20Z Adsorption of aqueous Hg2+ and inhibition of Hg0 re-emission from actual seawater flue gas desulfurization wastewater by using sulfurized activated carbon and NaClO Hsu C.-J;Chen Y.-H;Hsi H.-C.; Hsu C.-J; Chen Y.-H; Hsi H.-C.; HSING-CHENG HSI
臺大學術典藏 2021-08-05T02:41:20Z A simulation study of mercury immobilization in estuary sediment microcosm by activated carbon/clay-based thin-layer capping under artificial flow and turbation Ting Y;Ch'ng B.-L;Chen C;Ou M.-Y;Cheng Y.-H;Hsu C.-J;Hsi H.-C.; Ting Y; Ch'ng B.-L; Chen C; Ou M.-Y; Cheng Y.-H; Hsu C.-J; Hsi H.-C.; HSING-CHENG HSI
臺大學術典藏 2021-07-26T10:01:32Z A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss Lin Y.-H;Lin Y.-H;Lu Y.-C;Liu T.-C;Chen C.-Y;Hsu C.-J;Chen P.-L;Wu C.-C.; Lin Y.-H; Lin Y.-H; Lu Y.-C; Liu T.-C; Chen C.-Y; Hsu C.-J; Chen P.-L; Wu C.-C.; CHIEN-YU CHEN
臺大學術典藏 2021-07-06T02:04:15Z Application of Massively Parallel Sequencing to Genetic Diagnosis in Multiplex Families with Idiopathic Sensorineural Hearing Impairment Wu C.-C.; Lin Y.-H.; Lu Y.-C.; Chen P.-J.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN
臺大學術典藏 2021-07-06T02:04:11Z Identification of a novel GATA3 mutation in a deaf Taiwanese family by massively parallel sequencing Lin Y.-H.; Wu C.-C.; Hsu T.-Y.; Chiu W.-Y.; Hsu C.-J.; PEI-LUNG CHEN
臺大學術典藏 2021-07-06T02:04:09Z Identifying children with poor cochlear implantation outcomes using massively parallel sequencing Wu C.-C.; Lin Y.-H.; Liu T.-C.; Lin K.-N.; Yang W.-S.; Hsu C.-J.; PEI-LUNG CHEN; Wu C.-M.
臺大學術典藏 2021-07-06T02:04:02Z A novel missense variant in the nuclear localization signal of POU4F3 causes autosomal dominant non-syndromic hearing loss Lin Y.-H.; Lin Y.-H.; Lu Y.-C.; Liu T.-C.; Chen C.-Y.; Hsu C.-J.; PEI-LUNG CHEN; Wu C.-C.
臺大學術典藏 2021-07-06T02:04:02Z Prediction Model for Audiological Outcomes in Patients with GJB2 Mutations Chen P.-Y.; Lin Y.-H.; Liu T.-C.; Lin Y.-H.; Tseng L.-H.; Yang T.-H.; PEI-LUNG CHEN; Wu C.-C.; Hsu C.-J.
臺大學術典藏 2021-07-06T02:03:57Z Targeted Next-Generation Sequencing Facilitates Genetic Diagnosis and Provides Novel Pathogenetic Insights into Deafness with Enlarged Vestibular Aqueduct Lin Y.-H.;Wu C.-C.;Lin Y.-H.;Lu Y.-C.;Chen C.-S.;Liu T.-C.;Pei-Lung Chen;Hsu C.-J.; Lin Y.-H.; Wu C.-C.; Lin Y.-H.; Lu Y.-C.; Chen C.-S.; Liu T.-C.; PEI-LUNG CHEN; Hsu C.-J.

Showing items 101-110 of 419  (42 Page(s) Totally)
<< < 6 7 8 9 10 11 12 13 14 15 > >>
View [10|25|50] records per page