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

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Showing items 316-325 of 2057 (206 Page(s) Totally)
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Institution	Date	Title	Author
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.

Showing items 316-325 of 2057 (206 Page(s) Totally)
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