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

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Showing items 71-80 of 422 (43 Page(s) Totally)
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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	2021-07-06T02:03:57Z	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	2021-07-05T05:41:53Z	Functional evaluation of therapeutic response of HCC827 lung cancer to bevacizumab and erlotinib targeted therapy using dynamic contrast-enhanced and diffusion-weighted MRI	Chen Y.-F.; Yuan A.; Cho K.-H.; Lu Y.-C.; YEN-PING KUO; Chen J.-H.; Chang Y.-C.
臺大學術典藏	2021-07-03T03:35:01Z	Prospective mutation screening of three common deafness genes in a large Taiwanese cohort with idiopathic bilateral sensorineural hearing impairment reveals a difference in the results between families from hospitals and those from rehabilitation facilities	Wu C.-C.; PEI-JER CHEN; Chiu Y.-H.; Lu Y.-C.; Wu M.-C.; Hsu C.-J.
臺大學術典藏	2021-07-03T03:34:55Z	Application of SNaPshot multiplex assays for simultaneous multigene mutation screening in patients with idiopathic sensorineural hearing impairment	Wu C.-C.; Lu Y.-C.; PEI-JER CHEN; Liu A.Y.-Z.; Hwu W.-L.; Hsu C.-J.
臺大學術典藏	2021-07-03T03:34:48Z	Mutations in the OTOF gene in Taiwanese patients with auditory neuropathy	Chiu Y.-H.; Wu C.-C.; Lu Y.-C.; PEI-JER CHEN; Lee W.-Y.; Liu A.Y.-Z.; Hsu C.-J.
臺大學術典藏	2021-07-03T03:34:45Z	Phenotypic analyses and mutation screening of the SLC26A4 and FOXI1 genes in 101 Taiwanese families with bilateral nonsyndromic enlarged vestibular aqueduct (DFNB4) or pendred syndrome	Wu C.-C.; Lu Y.-C.; PEI-JER CHEN; Yeh P.-L.; Su Y.-N.; Hwu W.-L.; Hsu C.-J.
臺大學術典藏	2021-07-03T03:34:39Z	Establishment of a knock-in mouse model with the SLC26A4 c.919-2a>G mutation and characterization of its pathology	Lu Y.-C.; Wu C.-C.; Shen W.-S.; Yang T.-H.; Yeh T.-H.; PEI-JER CHEN; Yu I.-S.; Lin S.-W.; Wong J.-M.; Chang Q.; Lin X.; Hsu C.-J.
臺大學術典藏	2021-07-03T03:34:17Z	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.; PEI-JER CHEN; Yang W.-S.; Hsu C.-J.; Chen P.-L.
臺大學術典藏	2021-07-03T03:34:00Z	Contribution of adiponectin and its type 1 receptor to age-related hearing impairment	Wu C.-C.; Tsai C.-H.; Lu Y.-C.; Lin H.-C.; Hwang J.-H.; Lin Y.-H.; Yang W.-S.; PEI-JER CHEN; Liao W.-C.; Lee Y.L.; Liu T.-C.; Hsu C.-J.

Showing items 71-80 of 422 (43 Page(s) Totally)
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