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

	English \| 正體中文 \| 简体中文 \| Total items :0
	Visitors : 50691287 Online Users : 366 Project Commissioned by the Ministry of Education Project Executed by National Taiwan University Library

Scope

Adv. Search

Login

Administrator

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

About TAIR
	About TAIR

Browse By
	Institution
	Author
	Title
	Date
	Statistics Chart
	Institution Facts
	Trend

News
	2019臺灣學術機構典藏研討會
	機構典藏系統RC7版本已發佈

Copyright
	Publisher & Journal Policy
	TAIR Copyright Conference Minutes

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

"wuh liang hwu"

Return to Browse by Author
Sorting by Title	Sort by Date

Showing items 126-135 of 458 (46 Page(s) Totally)
<< < 8 9 10 11 12 13 14 15 16 17 > >>
View [10|25|50] records per page

Institution	Date	Title	Author
臺大學術典藏	2020-12-16T02:26:14Z	Poor outcome for neonatal-type nonketotic hyperglycinemia treated with high-dose sodium benzoate and dextromethorphan	Chien Y.-H.;Hsu C.-C.;Huang A.;Chou S.-P.;Lu F.-L.;Lee W.-T.;Wuh-Liang Hwu; Chien Y.-H.; Hsu C.-C.; Huang A.; Chou S.-P.; Lu F.-L.; Lee W.-T.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:14Z	Mutation spectrum in Taiwanese patients with phenylalanine hydroxylase deficiency and a founder effect for the R241C mutation.	Chien Y.H.;Chiang S.C.;Huang A.;Chou S.P.;Tseng S.S.;Huang Y.T.;Wuh-Liang Hwu; Chien Y.H.; Chiang S.C.; Huang A.; Chou S.P.; Tseng S.S.; Huang Y.T.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:14Z	Phenotype and genotype analyses of ornithine transcarbamylase deficiency in Taiwanese	Huang Y.-T.;Chien Y.-H.;Yeh H.-Y.;Lin S.-J.;Lu F.L.;Chou S.-P.;Lin J.-M.;Chiang S.-H.;Wuh-Liang Hwu; Huang Y.-T.; Chien Y.-H.; Yeh H.-Y.; Lin S.-J.; Lu F.L.; Chou S.-P.; Lin J.-M.; Chiang S.-H.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:13Z	Gene symbol: WAS. Disease: Wiskott-Aldrich syndrome.	Chien Y.H.;Wuh-Liang Hwu; Chien Y.H.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:13Z	Gene symbol: WAS. Disease: Wiskott-Aldrich syndrome.	Chien Y.H.;Wuh-Liang Hwu;Ariga T.; Chien Y.H.; WUH-LIANG HWU; Ariga T.
臺大學術典藏	2020-12-16T02:26:13Z	RNF4 is a coactivator for nuclear factor Y on GTP cyclohydrolase I proximal promoter	Wu S.-M.;Kuo W.-C.;Wuh-Liang Hwu;Hwa K.-Y.;Mantovani R.;Lee Y.-M.; Wu S.-M.; Kuo W.-C.; WUH-LIANG HWU; Hwa K.-Y.; Mantovani R.; Lee Y.-M.
臺大學術典藏	2020-12-16T02:26:13Z	Gene symbol: WAS. Disease: Wiskott-Aldrich syndrome.	Chien Y.H.;Wuh-Liang Hwu;Ariga T.; Chien Y.H.; WUH-LIANG HWU; Ariga T.
臺大學術典藏	2020-12-16T02:26:12Z	Partial trisomy 1 with congenital hydrocephalus and hypogammaglobulinemia: Report of one case	Wuh-Liang Hwu;Kuo P.-L.;Hung Y.-T.;Chien Y.-H.;Chu S.-Y.; WUH-LIANG HWU; Kuo P.-L.; Hung Y.-T.; Chien Y.-H.; Chu S.-Y.
臺大學術典藏	2020-12-16T02:26:12Z	A step-wise diagnosis of fragile X syndrome in Taiwan	Huang Y.-T.;Chiang S.-C.;Tzeng C.-C.;Liu C.-H.;Chien Y.-H.;Wuh-Liang Hwu; Huang Y.-T.; Chiang S.-C.; Tzeng C.-C.; Liu C.-H.; Chien Y.-H.; WUH-LIANG HWU
臺大學術典藏	2020-12-16T02:26:12Z	Detection of a homozygous D645E mutation of the acid α-glucosidase gene and glycogen deposition in tissues in a second-trimester fetus with infantile glycogen storage disease type II [3]	Chen C.-P.;Lin S.-P.;Tzen C.-Y.;Tsai F.-J.;Wuh-Liang Hwu;Wang W.; Chen C.-P.; Lin S.-P.; Tzen C.-Y.; Tsai F.-J.; WUH-LIANG HWU; Wang W.

Showing items 126-135 of 458 (46 Page(s) Totally)
<< < 8 9 10 11 12 13 14 15 16 17 > >>
View [10|25|50] records per page