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

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Institution	Date	Title	Author
臺大學術典藏	2020-12-16T02:25:38Z	Multimodel assessment of BRCA1 mutations in Taiwanese (ethnic Chinese) women with early-onset, bilateral or familial breast cancer	Kuo W.-H.; Lin P.-H.; Huang A.-C.; Chien Y.-H.; Liu T.-P.; Lu Y.-S.; Bai L.-Y.; Sargeant A.M.; Lin C.-H.; Cheng A.-L.; Hsieh F.-J.; WUH-LIANG HWU; Chang K.-J.
臺大學術典藏	2020-12-16T02:25:27Z	Cyclic pamidronate infusion for neonatal-onset Osteogenesis imperfecta	Lin C.-H.; Chien Y.-H.; Peng S.-F.; Tsai W.-Y.; Tung Y.-C.; Lee C.-T.; Chien C.-C.; WUH-LIANG HWU; Lee N.-C.
臺大學術典藏	2020-12-16T02:25:04Z	Heterogeneous nonataxic phenotypes of spinocerebellar ataxia in a Taiwanese population	Chen S.-J.;Lee N.-C.;Chien Y.-H.;Wuh-Liang Hwu;Lin C.-H.; Chen S.-J.; Lee N.-C.; Chien Y.-H.; WUH-LIANG HWU; Lin C.-H.
臺大學術典藏	2020-12-09T05:58:47Z	Akt suppresses DLK for maintaining self-renewal of mouse embryonic stem cells	Wu C.-C.; Wu H.-J.; Wang C.-H.; Lin C.-H.; Hsu S.-C.; Chen Y.-R.; Hsiao M.; Schuyler S.C.; FRANK LEIGH LU; Ma N.; Lu J.
臺大學術典藏	2020-12-09T01:38:20Z	A limb-girdle myopathy phenotype of RUNX2 mutation in a patient with cleidocranial dysplasia: A case study and literature review	Yang S.-H.; Lin H.-I.; Lin C.-H.; NI-CHUNG LEE; Hsueh S.-J.; Hsueh S.-J.;Ni-Chung Lee;Yang S.-H.;Lin H.-I.;Lin C.-H.
臺大學術典藏	2020-12-09T01:38:10Z	Heterogeneous nonataxic phenotypes of spinocerebellar ataxia in a Taiwanese population	Chen S.-J.;Ni-Chung Lee;Chien Y.-H.;Hwu W.-L.;Lin C.-H.; Chen S.-J.; NI-CHUNG LEE; Chien Y.-H.; Hwu W.-L.; Lin C.-H.
臺大學術典藏	2020-12-09T01:38:07Z	Clinical and electrophysiological characteristics of a type 1 sialidosis patient with a novel deletion mutation in NEU1 gene	Fan S.-P.; NI-CHUNG LEE; Lin C.-H.
臺大學術典藏	2020-12-09T01:38:05Z	Clinical, radiological, and genetic characteristics in patients with Huntington's disease in a Taiwanese cohort	Chen S.-J.;Lee B.-C.;Ni-Chung Lee;Chien Y.-H.;Hwu W.-L.;Lin C.-H.; Chen S.-J.; Lee B.-C.; NI-CHUNG LEE; Chien Y.-H.; Hwu W.-L.; Lin C.-H.
臺大學術典藏	2020-12-09T01:38:05Z	Novel Phenotype of 6p25 Deletion Syndrome Presenting Juvenile Parkinsonism and Brain Calcification	Fan S.-P.;Ni-Chung Lee;Lin C.-H.; Fan S.-P.; NI-CHUNG LEE; Lin C.-H.
臺大學術典藏	2020-12-07T07:12:07Z	Better adherence to the guidelines during cardiopulmonary resuscitation through the provision of audio-prompts	Chiang W.-C.; Chen W.-J.; Chen S.-Y.; Ko P.C.-I.; Lin C.-H.; Tsai M.-S.; Chang W.-T.; SHYR-CHYR CHEN; Tsan C.-Y.; Ma M.H.-M.

Showing items 946-955 of 3227 (323 Page(s) Totally)
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