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Showing items 156-180 of 715 (29 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2021-01-27T01:38:19Z	Quantitative analysis of SMN1 and SMN2 genes based on DHPLC: A highly efficient and reliable carrier-screening test	Su Y.-N.;Hung C.-C.;Li H.;Lee C.-N.;Cheng W.-F.;Tsao P.-N.;Chang M.-C.;Chia-Li Yu;Hsieh W.-S.;Lin W.-L.;Hsu S.-M.; Su Y.-N.; Hung C.-C.; Li H.; Lee C.-N.; Cheng W.-F.; Tsao P.-N.; Chang M.-C.; CHIA-LI YU; Hsieh W.-S.; Lin W.-L.; Hsu S.-M.
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	Excess soluble fms-like tyrosine kinase 1 and low platelet counts in premature neonates of preeclamptic mothers	Tsao P.-N.;Wei S.-C.;Su Y.-N.;Chou H.-C.;Chien-Yi Chen;Hsieh W.-S.; Tsao P.-N.; Wei S.-C.; Su Y.-N.; Chou H.-C.; CHIEN-YI CHEN; Hsieh W.-S.
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.
臺大學術典藏	2021-01-21T02:05:07Z	Congenital central hypoventilation syndrome with PHOX2B gene mutation in a Taiwanese infant	Chen L.-R.;Tsao P.-N.;Su Y.-N.;Fan P.-C.;Chou H.-C.;Chien-Yi Chen;Chang Y.-H.;Hsieh W.-S.; Chen L.-R.; Tsao P.-N.; Su Y.-N.; Fan P.-C.; Chou H.-C.; CHIEN-YI CHEN; Chang Y.-H.; Hsieh W.-S.
臺大學術典藏	2021-01-21T02:05:06Z	Holt-Oram syndrome with right lung agenesis caused by a de novo mutation in the TBX5 gene [2]	Tseng Y.-R.;Su Y.-N.;Lu F.L.;Jeng S.-F.;Hsieh W.-S.;Chien-Yi Chen;Chou H.-C.;Peng S.S.-F.; Tseng Y.-R.; Su Y.-N.; Lu F.L.; Jeng S.-F.; Hsieh W.-S.; CHIEN-YI CHEN; Chou H.-C.; Peng S.S.-F.
臺大學術典藏	2021-01-21T02:05:06Z	Soluble vascular endothelial growth factor receptor-1 protects mice in sepsis	Tsao P.-N.;Chan F.-T.;Wei S.-C.;Hsieh W.-S.;Chou H.-C.;Su Y.-N.;Chien-Yi Chen;Hsu W.-M.;Hsieh F.-J.;Hsu S.-M.; Tsao P.-N.; Chan F.-T.; Wei S.-C.; Hsieh W.-S.; Chou H.-C.; Su Y.-N.; CHIEN-YI CHEN; Hsu W.-M.; Hsieh F.-J.; Hsu S.-M.
臺大學術典藏	2021-01-21T02:05:05Z	Neonatal and Pregnancy Outcome in Primary Antiphospholipid Syndrome: A 10-year Experience in One Medical Center	Chou A.-K.; Hsieh S.-C.; Su Y.-N.; Jeng S.-F.; CHIEN-YI CHEN; Chou H.-C.; Tsao P.-N.; Hsieh W.-S.
臺大學術典藏	2021-01-21T02:05:02Z	211 G to A variation of UDP-glucuronosyl transferase 1A1 gene and neonatal Breastfeeding jaundice	Chou H.-C.;Chen M.-H.;Yang H.-I.;Su Y.-N.;Hsieh W.-S.;Chien-Yi Chen;Chen H.-L.;Chang M.-H.;Tsao P.-N.; Chou H.-C.; Chen M.-H.; Yang H.-I.; Su Y.-N.; Hsieh W.-S.; CHIEN-YI CHEN; Chen H.-L.; Chang M.-H.; Tsao P.-N.
臺大學術典藏	2021-01-21T02:05:01Z	Novel heterozygous tissue-nonspecific alkaline phosphatase (TNAP) gene mutations causing lethal perinatal hypophosphatasia	Chang K.-C.; Lin P.-H.; Su Y.-N.; Peng S.S.-F.; Lee N.-C.; Chou H.-C.; CHIEN-YI CHEN; Hsieh W.-S.; Tsao P.-N.
臺大學術典藏	2021-01-21T02:04:51Z	The sFlt-1/PlGF ratio as a predictor for poor pregnancy and neonatal outcomes	Chang Y.-S.;Chen C.-N.;Jeng S.-F.;Su Y.-N.;Chien-Yi Chen;Chou H.-C.;Tsao P.-N.;Hsieh W.-S.; Chang Y.-S.; Chen C.-N.; Jeng S.-F.; Su Y.-N.; CHIEN-YI CHEN; Chou H.-C.; Tsao P.-N.; Hsieh W.-S.
臺大學術典藏	2021-01-15T02:46:30Z	Neonatal and Pregnancy Outcome in Primary Antiphospholipid Syndrome: A 10-year Experience in One Medical Center	Chou A.-K.; SONG-CHOU HSIEH; Su Y.-N.; Jeng S.-F.; Chen C.-Y.; Chou H.-C.; Tsao P.-N.; Hsieh W.-S.
臺大學術典藏	2021-01-15T02:46:26Z	A whole genome methylation analysis of systemic lupus erythematosus: Hypomethylation of the IL10 and IL1R2 promoters is associated with disease activity	Lin S.-Y.; SONG-CHOU HSIEH; Lin Y.-C.; Lee C.-N.; Tsai M.-H.; Lai L.-C.; Chuang E.Y.; Chen P.-C.; Hung C.-C.; Chen L.-Y.; Hsieh W.S.; Niu D.-M.; Su Y.-N.; Ho H.-N.
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	2021-01-08T07:28:12Z	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	2021-01-08T06:17:24Z	Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome	Lin S.-Y.;Lee C.-N.;Hung C.-C.;Tsai W.-Y.;Lin S.-P.;Li N.-C.;Hsieh W.-S.;Yi-Ching Tung;Niu D.-M.;Hsu W.-M.;Chen L.-Y.;Fang M.-Y.;Tu M.-P.;Kuo P.-W.;Lin C.-Y.;Su Y.-N.;Ho H.-N.; Lin S.-Y.; Lee C.-N.; Hung C.-C.; Tsai W.-Y.; Lin S.-P.; Li N.-C.; Hsieh W.-S.; YI-CHING TUNG; Niu D.-M.; Hsu W.-M.; Chen L.-Y.; Fang M.-Y.; Tu M.-P.; Kuo P.-W.; Lin C.-Y.; Su Y.-N.; Ho H.-N.
臺大學術典藏	2021-01-08T06:17:19Z	Mosaic paternal haploidy in a patient with pancreatoblastoma and Beckwith–Wiedemann spectrum	Lee C.-T.;Yi-Ching Tung;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.; Lee C.-T.; YI-CHING TUNG; 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	2021-01-08T02:16:01Z	Concurrent Hearing, Genetic, and Cytomegalovirus Screening in Newborns, Taiwan	Lin Y.-H.; Ke Y.-Y.; Tsao P.-N.; CHUN-YI LU; Chun-Yi Lu;Tsao P.-N.;Ke Y.-Y.;Lin Y.-H.;Lin Y.-H.;Hung C.-C.;Su Y.-N.;Hsu W.-C.;Hsieh W.-S.;Huang L.-M.;Wu C.-C.;Hsu C.-J.; Hsu C.-J.; Lin Y.-H.; Hung C.-C.; Su Y.-N.; Hsu W.-C.; Hsieh W.-S.; Huang L.-M.; Wu C.-C.
臺大學術典藏	2021-01-06T05:46:48Z	Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases	Lee C.-N.;Su Y.-N.;Cheng W.-F.;Lin M.-T.;Jou-Kou Wang;Wu M.-H.;Hsieh F.-J.; Lee C.-N.; Su Y.-N.; Cheng W.-F.; Lin M.-T.; JOU-KOU WANG; Wu M.-H.; Hsieh F.-J.
臺大學術典藏	2021-01-06T03:39:08Z	IKZF1 deletions predict a poor prognosis in children with B-cell progenitor acute lymphoblastic leukemia: A multicenter analysis in Taiwan	Jou S.-T.; Hsiao C.-C.; Sheen J.-M.; Cheng C.-N.; Wu K.-H.; Lin S.-R.; Yu S.-L.; Chen H.-Y.; Lu M.-Y.; Wang S.-C.; Chang H.-H.; Lin S.-W.; Su Y.-N.; Lin D.-T.; YUNG-LI YANG; Hung C.-C.; Chen J.-S.; Lin K.-H.
臺大學術典藏	2021-01-06T03:38:55Z	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.; YUNG-LI YANG; 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	2021-01-06T03:38:54Z	TP53 alterations in relapsed childhood acute lymphoblastic leukemia	Lin K.-H.; Lin C.-Y.; Lin T.-K.; Chang Y.-H.; Jou S.-T.; Chang W.-T.; Yu C.-H.; Lu M.-Y.; Chen S.-H.; Wu K.-H.; Wang S.-C.; Chang H.-H.; Su Y.-N.; Hung C.-C.; Lin D.-T.; Chen H.-Y.; YUNG-LI YANG
臺大學術典藏	2021-01-06T03:38:51Z	MLPA and DNA index improve the molecular diagnosis of childhood B-cell acute lymphoblastic leukemia	Lu M.-Y.; Chen S.-H.; Cheng C.-N.; Wu K.-H.; Wang S.-C.; Chang H.-H.; Li M.-J.; Ni Y.-L.; Su Y.-N.; Lin D.-T.; Chen H.-Y.; Harrison C.J.; Hung C.-C.; Lin S.-W.; YUNG-LI YANG; Yu C.-H.; Lin T.-K.; Jou S.-T.; Lin C.-Y.; Lin K.-H.
臺大學術典藏	2021-01-05T08:07:44Z	Denaturing high-performance liquid chromatography screening of the long QT syndrome-related cardiac sodium and potassium channel genes and identification of novel mutations and single nucleotide polymorphisms	Lo H.-M.; Huang S.K.S.; Lin J.-L.; Lai L.-P.;Su Y.-N.;Chiang F.-T.;Juang J.-M.;Liu Y.-B.;Ho Y.-L.;Chen W.-J.;Yeh S.-J.;Wang C.-C.;Ko Y.-L.;Wu T.-J.;Ueng K.-C.;Lei M.-H.;Tsao H.-M.;Chen S.-A.;Lin T.-K.;Mei-Hwan Wu;Lo H.-M.;Huang S.K.S.;Lin J.-L.; Lai L.-P.; Su Y.-N.; Chiang F.-T.; Juang J.-M.; Liu Y.-B.; Ho Y.-L.; Chen W.-J.; Yeh S.-J.; Wang C.-C.; Ko Y.-L.; Wu T.-J.; Ueng K.-C.; Lei M.-H.; Tsao H.-M.; Chen S.-A.; Lin T.-K.; MEI-HWAN WU
臺大學術典藏	2021-01-05T08:07:39Z	Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases	Lee C.-N.;Su Y.-N.;Cheng W.-F.;Lin M.-T.;Wang J.-K.;Mei-Hwan Wu;Hsieh F.-J.; Lee C.-N.; Su Y.-N.; Cheng W.-F.; Lin M.-T.; Wang J.-K.; MEI-HWAN WU; Hsieh F.-J.

Showing items 156-180 of 715 (29 Page(s) Totally)
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