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

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Showing items 661-670 of 2819 (282 Page(s) Totally)
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Institution	Date	Title	Author
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	2021-07-06T02:04:07Z	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	2021-07-06T02:04:04Z	Clinical heterogeneity of LRRK2 p.I2012T mutation	Fan T.-S.;Wu R.-M.;Pei-Lung Chen;Chen T.-F.;Li H.-Y.;Lin Y.-H.;Chen C.-Y.;Chen M.-L.;Tai C.-H.;Lin H.-I.;Lin C.-H.; Fan T.-S.; Wu R.-M.; PEI-LUNG CHEN; Chen T.-F.; Li H.-Y.; Lin Y.-H.; Chen C.-Y.; Chen M.-L.; Tai C.-H.; Lin H.-I.; Lin C.-H.
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.

Showing items 661-670 of 2819 (282 Page(s) Totally)
<< < 62 63 64 65 66 67 68 69 70 71 > >>
View [10|25|50] records per page