臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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臺灣學術機構典藏系統 (Taiwan Academic Institutional Repository, TAIR)

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Institution	Date	Title	Author
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	2021-07-06T02:04:00Z	ABO genotyping with next-generation sequencing to resolve heterogeneity in donors with serology discrepancies	Wu P.C.; Lin Y.-H.; Tsai L.F.; Chen M.H.; PEI-LUNG CHEN; Pai S.-C.
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.
臺大學術典藏	2021-07-06T02:03:57Z	Unique spectra of deafness-associated mutations in Mongolians provide insights into the genetic relationships among Eurasian populations	Erdenechuluun J.; Lin Y.-H.; Ganbat K.; Bataakhuu D.; Makhbal Z.; Tsai C.-Y.; Lin Y.-H.; Chan Y.-H.; Hsu C.-J.; Hsu W.-C.; PEI-LUNG CHEN; Wu C.-C.
臺大學術典藏	2021-07-06T02:03:56Z	P53 ICE CRIM mouse: A tool to generate mutant allelic series in somatic cells and germ lines for cancer studies	Fan H.-H.;Shing Yu I.;Lin Y.-H.;Wang S.-Y.;Liaw Y.-H.;Pei-Lung Chen;Yang T.-L.;Lin S.-W.;Chen Y.-T.; Fan H.-H.; Shing Yu I.; Lin Y.-H.; Wang S.-Y.; Liaw Y.-H.; PEI-LUNG CHEN; Yang T.-L.; Lin S.-W.; Chen Y.-T.
臺大學術典藏	2021-07-06T02:03:53Z	Genetic epidemiology and clinical features of hereditary hearing impairment in the Taiwanese population	Wu C.-C.;Tsai C.-Y.;Lin Y.-H.;Chen P.-Y.;Lin P.-H.;Cheng Y.-F.;Wu C.-M.;Lin Y.-H.;Lee C.-Y.;Erdenechuluun J.;Liu T.-C.;Pei-Lung Chen;Hsu C.-J.; Wu C.-C.; Tsai C.-Y.; Lin Y.-H.; Chen P.-Y.; Lin P.-H.; Cheng Y.-F.; Wu C.-M.; Lin Y.-H.; Lee C.-Y.; Erdenechuluun J.; Liu T.-C.; PEI-LUNG CHEN; Hsu C.-J.
臺大學術典藏	2021-07-06T02:03:49Z	An integrative approach for pediatric auditory neuropathy spectrum disorders: revisiting etiologies and exploring the prognostic utility of auditory steady-state response	Lin P.-H.; Hsu C.-J.; Lin Y.-H.; Lin Y.-H.; Yang S.-Y.; Yang T.-H.; PEI-LUNG CHEN; Wu C.-C.; Liu T.-C.
臺大學術典藏	2021-07-06T02:03:47Z	Next-generation sequencing and bioinformatics to identify genetic causes of malignant hyperthermia	Yeh H.-M.; Liao M.-H.; Chu C.-L.; Lin Y.-H.; Sun W.-Z.; Lai L.-P.; PEI-LUNG CHEN
臺大學術典藏	2021-07-05T07:59:12Z	Toxic mechanisms of Roth801, Canals, microparticles and nanoparticles of ZnO on MG-63 osteoblasts	Chang M.-C.; Tang C.-M.; Lin Y.-H.; Liu H.-C.; Wang T.-M.; Lan W.-C.; Cheng R.-H.; Lin Y.-R.; HSIAO-HUA CHANG; Jeng J.-H.

Showing items 666-675 of 2819 (282 Page(s) Totally)
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