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教育部委託研究計畫      計畫執行:國立臺灣大學圖書館
 
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機構 日期 題名 作者
臺大學術典藏 2021-07-03T03:35:26Z Specificity of SLC26A4 mutations in the pathogenesis of inner ear malformations Wu C.-C.; PEI-JER CHEN; Hsu C.-J.
臺大學術典藏 2021-07-03T03:35:25Z Prevalent SLC26A4 mutations in patients with enlarged vestibular aqueduct and/or Mondini dysplasia: A unique spectrum of mutations in Taiwan, including a frequent founder mutation Wu C.-C.; Yeh T.-H.; PEI-JER CHEN; Hsu C.-J.
臺大學術典藏 2021-07-03T03:35:23Z Common clinical features of children with enlarged vestibular aqueduct and mondini dysplasia Wu C.-C.; Chen Y.-S.; PEI-JER CHEN; Hsu C.-J.
臺大學術典藏 2021-07-03T03:35:08Z Prevalence and clinical features of the mitochondrial m.1555A>G mutation in Taiwanese patients with idiopathic sensorineural hearing loss and association of haplogroup F with low penetrance in three families Wu C.-C.; Chiu Y.-H.; PEI-JER CHEN; Hsu C.-J.
臺大學術典藏 2021-07-03T03:35:03Z Predominance of genetic diagnosis and imaging results as predictors in determining the speech perception performance outcome after cochlear implantation in children Wu C.-C.; Lee Y.-C.; PEI-JER CHEN; Hsu C.-J.
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 2021-07-03T03:34:53Z Heparanase inhibitor PI-88 as adjuvant therapy for hepatocellular carcinoma after curative resection: A randomized phase II trial for safety and optimal dosage Liu C.-J.; Lee P.-H.; Lin D.-Y.; Wu C.-C.; Jeng L.-B.; Lin P.-W.; Mok K.-T.; Lee W.-C.; Yeh H.-Z.; Ho M.-C.; Yang S.-S.; Lee C.-C.; Yu M.-C.; Hu R.-H.; Peng C.-Y.; Lai K.-L.; Chang S.S.-C.; PEI-JER CHEN
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.

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