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

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機構	日期	題名	作者
臺大學術典藏	2021-02-04T06:05:16Z	Pulmonary embolism due to protein S deficiency in pregnancy	Mak P.-H.;Shyu M.-K.;Chien-Nan Lee;Hsieh F.-J.; Mak P.-H.; Shyu M.-K.; CHIEN-NAN LEE; Hsieh F.-J.
臺大學術典藏	2021-02-04T06:05:15Z	Molecular genetic analysis of the TSC genes in two families with prenatally diagnosed rhabdomyomas [1]	Chen C.-P.;Su Y.-N.;Hung C.-C.;Chien-Nan Lee;Hsieh F.-J.;Chang T.-Y.;Chen M.-R.;Wang W.; Chen C.-P.; Su Y.-N.; Hung C.-C.; CHIEN-NAN LEE; Hsieh F.-J.; Chang T.-Y.; Chen M.-R.; Wang W.
臺大學術典藏	2021-02-04T06:05:14Z	Hypoxia-induced apoptosis in endothelial cells and embryonic stem cells	Chien-Nan Lee;Cheng W.-F.;Chang M.-C.;Su Y.-N.;Chen C.-A.;Hsieh F.-J.; CHIEN-NAN LEE; Cheng W.-F.; Chang M.-C.; Su Y.-N.; Chen C.-A.; Hsieh F.-J.
臺大學術典藏	2021-02-04T06:05:13Z	Isolated right diaphragmatic eventration mimicking congenital heart disease in utero	Yang C.-K.;Shih J.-C.;Hsu W.-M.;Peng S.-S.;Shyu M.-K.;Chien-Nan Lee;Hsieh F.-J.; Yang C.-K.; Shih J.-C.; Hsu W.-M.; Peng S.-S.; Shyu M.-K.; CHIEN-NAN LEE; Hsieh F.-J.
臺大學術典藏	2021-02-04T06:05:12Z	Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases	Chien-Nan Lee;Su Y.-N.;Cheng W.-F.;Lin M.-T.;Wang J.-K.;Wu M.-H.;Hsieh F.-J.; CHIEN-NAN LEE; Su Y.-N.; Cheng W.-F.; Lin M.-T.; Wang J.-K.; Wu M.-H.; Hsieh F.-J.
臺大學術典藏	2021-02-04T06:05:06Z	Mucin 15 is expressed in human placenta and suppresses invasion of trophoblast-like cells in vitro	Shyu M.-K.;Lin M.-C.;Shih J.-C.;Chien-Nan Lee;Huang J.;Liao C.-H.;Huang I.-F.;Chen H.-Y.;Huang M.-C.;Hsieh F.-J.; Shyu M.-K.; Lin M.-C.; Shih J.-C.; CHIEN-NAN LEE; Huang J.; Liao C.-H.; Huang I.-F.; Chen H.-Y.; Huang M.-C.; Hsieh F.-J.
臺大學術典藏	2021-02-04T06:05:05Z	Polymorphisms in the endothelial nitric oxide synthase gene may be protective against preeclampsia in a Chinese population	Chen L.-K.;Huang C.-H.;Yeh H.-M.;Chien-Nan Lee;Shyu M.-K.;Hsieh F.-J.;Lai L.-P.;Sun W.-Z.; Chen L.-K.; Huang C.-H.; Yeh H.-M.; CHIEN-NAN LEE; Shyu M.-K.; Hsieh F.-J.; Lai L.-P.; Sun W.-Z.
臺大學術典藏	2021-01-27T01:38:22Z	Rapid detection of β-globin gene (HBB) mutations coupling heteroduplex and primer-extension analysis by DHPLC	Su Y.-N.;Lee C.-N.;Hung C.-C.;Chen C.-A.;Cheng W.-F.;Tsao P.-N.;Chia-Li Yu;Hsieh F.-J.; Su Y.-N.; Lee C.-N.; Hung C.-C.; Chen C.-A.; Cheng W.-F.; Tsao P.-N.; CHIA-LI YU; Hsieh F.-J.
臺大學術典藏	2021-01-27T01:38:18Z	Identification of forty-five novel and twenty-three known NF1 mutations in Chinese patients with neurofibromatosis type 1.	Lee M.J.; Su Y.N.; You H.L.; Chiou S.C.; Lin L.C.; Yang C.C.; Lee W.C.; Hwu W.L.; Hsieh F.J.; Stephenson D.A.; CHIA-LI YU
臺大學術典藏	2021-01-21T02:05:10Z	Vascular endothelial growth factor in preterm infants with respiratory distress syndrome	Tsao P.-N.;Wei S.-C.;Chou H.-C.;Su Y.-N.;Chien-Yi Chen;Hsieh F.-J.;Hsieh W.-S.; Tsao P.-N.; Wei S.-C.; Chou H.-C.; Su Y.-N.; CHIEN-YI CHEN; Hsieh F.-J.; Hsieh W.-S.

顯示項目 211-220 / 994 (共100頁)
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