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Showing items 296-305 of 2057  (206 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2021-07-06T02:04:15Z Common genetic mutations in the start codon of the SDH subunit D gene among Chinese families with familial head and neck paragangliomas Wang C.-P.; Chen T.-C.; Chang Y.-L.; Ko J.-Y.; Yang T.-L.; Lo F.-Y.; Hu Y.-L.; PEI-LUNG CHEN; Wu C.-C.; Lou P.-J.
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 2021-07-06T02:04:07Z Long-term cochlear implant outcomes in children with GJB2 and SLC26A4 mutations Wu C.-M.; Ko H.-C.; Tsou Y.-T.; Lin Y.-H.; Lin J.-L.; Chen C.-K.; PEI-LUNG CHEN; Wu C.-C.
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.
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 2021-07-06T02:03:53Z 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.

Showing items 296-305 of 2057  (206 Page(s) Totally)
<< < 25 26 27 28 29 30 31 32 33 34 > >>
View [10|25|50] records per page