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Showing items 216-225 of 419  (42 Page(s) Totally)
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Institution Date Title Author
臺大學術典藏 2020-04-24T01:34:25Z Association of central obesity with the severity and audiometric configurations of age-related hearing impairment Hwang J.-H.; Chen-Chi Wu; Hsu C.-J.; Liu T.-C.; Yang W.-S.
臺大學術典藏 2020-04-24T01:34:25Z Application of SNaPshot multiplex assays for simultaneous multigene mutation screening in patients with idiopathic sensorineural hearing impairment Chen-Chi Wu; Lu Y.-C.; Chen P.-J.; Liu A.Y.-Z.; Hwu W.-L.; Hsu C.-J.
臺大學術典藏 2020-04-24T01:34:25Z Mutations in the OTOF gene in Taiwanese patients with auditory neuropathy Chiu Y.-H.; Chen-Chi Wu; Lu Y.-C.; Chen P.-J.; Lee W.-Y.; Liu A.Y.-Z.; Hsu C.-J.
臺大學術典藏 2020-04-24T01:34:24Z Genetic characteristics in children with cochlear implants and the corresponding auditory performance Chen-Chi Wu; Liu T.-C.; Wang S.-H.; Hsu C.-J.; Wu C.-M.
臺大學術典藏 2020-04-24T01:34:24Z Establishment of a knock-in mouse model with the SLC26A4 c.919-2a>G mutation and characterization of its pathology Hsu C.-J.; Lu Y.-C.; Chen-Chi Wu; Shen W.-S.; Yang T.-H.; Yeh T.-H.; Chen P.-J.; Yu I.-S.; Lin S.-W.; Wong J.-M.; Chang Q.; Lin X.
臺大學術典藏 2020-04-24T01:34:24Z Preimplantation genetic diagnosis (embryo screening) for enlarged vestibular aqueduct due to SLC26A4 mutation Chen-Chi Wu; Lin S.-Y.; Su Y.-N.; Fang M.-Y.; Chen S.-U.; Hsu C.-J.
臺大學術典藏 2020-04-24T01:34:23Z Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome Wang S.-H.; Chen-Chi Wu; Lu Y.-C.; Lin Y.-H.; Su Y.-N.; Hwu W.-L.; Yu I.-S.; Hsu C.-J.
臺大學術典藏 2020-04-24T01:34:23Z Newborn genetic screening for hearing impairment: A preliminary study at a tertiary center Chen-Chi Wu; Hung C.-C.; Lin S.-Y.; Hsieh W.-S.; Tsao P.-N.; Lee C.-N.; Su Y.-N.; Hsu C.-J.
臺大學術典藏 2020-04-24T01:34:22Z In response to determinants of bilateral audiometric notches in noise-induced hearing loss Hsu T.-Y.; Chen-Chi Wu; Hsu C.-J.; Chang J.-G.; Lee S.-Y.
臺大學術典藏 2020-04-24T01:34:22Z Differences in the Pathogenicity of the p.H723R Mutation of the Common Deafness-Associated SLC26A4 Gene in Humans and Mice Wong J.-M.; Lin X.; Lu Y.-C.; Chen-Chi Wu; Yang T.-H.; Lin Y.-H.; Yu I.-S.; Lin S.-W.; Chang Q.; Hsu C.-J.

Showing items 216-225 of 419  (42 Page(s) Totally)
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