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機構 日期 題名 作者
臺大學術典藏 2021-01-11T07:19:40Z Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum Lee C.-T.; Tung Y.-C.; Hwu W.-L.; Shih J.-C.; Lin W.-H.; Wu M.-Z.; Kuo K.-T.; Yang Y.-L.; Chen H.-L.; Chen M.; Su Y.-N.; Jong Y.-J.; SHIH-YAO LIU; Tsai W.-Y.; Lee N.-C.
臺大學術典藏 2021-01-08T07:28:13Z Clinical characteristics of Taiwanese children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency detected by neonatal screening Liu S.-Y.;Cheng-Ting Lee;Tung Y.-C.;Chien Y.-H.;Hwu W.-L.;Tsai W.-Y.; Liu S.-Y.; CHENG-TING LEE; Tung Y.-C.; Chien Y.-H.; Hwu W.-L.; Tsai W.-Y.
臺大學術典藏 2021-01-08T07:28:13Z Cyclic pamidronate infusion for neonatal-onset Osteogenesis imperfecta Hwu W.-L.; Lee N.-C.; Chien C.-C.; Lin C.-H.;Chien Y.-H.;Peng S.-F.;Tsai W.-Y.;Tung Y.-C.;Cheng-Ting Lee;Chien C.-C.;Hwu W.-L.;Lee N.-C.; Lin C.-H.; Chien Y.-H.; Peng S.-F.; Tsai W.-Y.; Tung Y.-C.; CHENG-TING LEE
臺大學術典藏 2021-01-08T07:28:12Z SHOX deficiency in short Taiwanese children: A single-center experience Tung Y.-C.;Lee N.-C.;Hwu W.-L.;Liu S.-Y.;Cheng-Ting Lee;Chien Y.-H.;Tsai W.-Y.; Tung Y.-C.; Lee N.-C.; Hwu W.-L.; Liu S.-Y.; CHENG-TING LEE; Chien Y.-H.; Tsai W.-Y.
臺大學術典藏 2021-01-08T07:28:12Z Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum Cheng-Ting Lee;Tung Y.-C.;Hwu W.-L.;Shih J.-C.;Lin W.-H.;Wu M.-Z.;Kuo K.-T.;Yang Y.-L.;Chen H.-L.;Chen M.;Su Y.-N.;Jong Y.-J.;Liu S.-Y.;Tsai W.-Y.;Lee N.-C.; CHENG-TING LEE; Tung Y.-C.; Hwu W.-L.; Shih J.-C.; Lin W.-H.; Wu M.-Z.; Kuo K.-T.; Yang Y.-L.; Chen H.-L.; Chen M.; Su Y.-N.; Jong Y.-J.; Liu S.-Y.; Tsai W.-Y.; Lee N.-C.
臺大學術典藏 2021-01-08T07:28:11Z Thyroid disorders in Taiwanese children with Down syndrome: The experience of a single medical center Liu M.-Y.;Cheng-Ting Lee;Lee N.-C.;Tung Y.-C.;Chien Y.-H.;Hwu W.-L.;Tsai W.-Y.; Liu M.-Y.; CHENG-TING LEE; Lee N.-C.; Tung Y.-C.; Chien Y.-H.; Hwu W.-L.; Tsai W.-Y.
臺大學術典藏 2021-01-08T06:17:26Z Slipped capital femoral epiphysis as a complication of growth hormone therapy. Wang S.Y.; YI-CHING TUNG; Tsai W.Y.; Chien Y.H.; Lee J.S.; Hwu W.L.
臺大學術典藏 2021-01-08T06:17:23Z Congenital hypopituitarism due to POU1F1 gene mutation Lee N.-C.;Tsai W.-Y.;Peng S.-F.;Yi-Ching Tung;Chien Y.-H.;Hwu W.-L.; Lee N.-C.; Tsai W.-Y.; Peng S.-F.; YI-CHING TUNG; Chien Y.-H.; Hwu W.-L.
臺大學術典藏 2021-01-08T06:17:20Z Comprehensive human leukocyte antigen genotyping of patients with type 1 diabetes mellitus in Taiwan Tsai W.-Y.; Chen P.-L.; Hwu W.-L.; Yang W.-S.; Chu C.-C.; Chang C.-C.; Fann C.S.-J.; YI-CHING TUNG; Yi-Ching Tung;Fann C.S.-J.;Chang C.-C.;Chu C.-C.;Yang W.-S.;Hwu W.-L.;Chen P.-L.;Tsai W.-Y.
臺大學術典藏 2021-01-08T06:17:20Z Clinical characteristics of Taiwanese children with congenital adrenal hyperplasia due to 21-hydroxylase deficiency detected by neonatal screening Liu S.-Y.;Lee C.-T.;Yi-Ching Tung;Chien Y.-H.;Hwu W.-L.;Tsai W.-Y.; Liu S.-Y.; Lee C.-T.; YI-CHING TUNG; Chien Y.-H.; Hwu W.-L.; Tsai W.-Y.

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