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

	English \| 正體中文 \| 简体中文 \| 總筆數 :2854037
	造訪人次 : 45292355 線上人數 : 1349 教育部委託研究計畫計畫執行:國立臺灣大學圖書館

搜尋範圍

進階搜尋

登入

管理

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

關於TAIR
	計畫說明

瀏覽
	典藏機構
	作者
	題名
	日期
	統計圖表
	機構即時統計
	學術趨勢

消息
	2019臺灣學術機構典藏研討會
	機構典藏系統RC7版本已發佈

著作權
	出版社及期刊政策查詢
	TAIR著作權會議記錄

相關連結
	機構典藏計畫網站
	ROAR
	OpenDOAR
	SHERPA
	OAIster
	JAIRO
	Ira
	DSPACE
	RWWR
	臺大學術典藏NTU Scholars

"wu c c"的相關文件

回到依作者瀏覽
依題名排序	依日期排序

顯示項目 316-325 / 2057 (共206頁)
<< < 27 28 29 30 31 32 33 34 35 36 > >>
每頁顯示[10|25|50]項目

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.

顯示項目 316-325 / 2057 (共206頁)
<< < 27 28 29 30 31 32 33 34 35 36 > >>
每頁顯示[10|25|50]項目