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Showing items 1-25 of 114 (5 Page(s) Totally) 1 2 3 4 5 > >> View [10|25|50] records per page
臺大學術典藏 |
2018-09-10T07:21:48Z |
Neonatal and Pregnancy Outcome in Primary Antiphospholipid Syndrome: A 10-year Experience in One Medical Center
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Chou, A.-K. and Hsieh, S.-C. and Su, Y.-N. and Jeng, S.-F. and Chen, C.-Y. and Chou, H.-C. and Tsao, P.-N. and Hsieh, W.-S.; Chou, AK;Hsieh, SC;Su, YN;Jeng, SF;Chen, CY;Chou, HC;Tsao, PN;Hsieh, WS.; Chou, AK; SUH-FANG JENG; WU-SHIUN HSIEH; Hsieh, SC; Su, YN; HUNG-CHIEH CHOU; PO-NIEN TSAO; Jeng, SF; CHIEN-YI CHEN; Chen, CY; Chou, HC; Tsao, PN; Hsieh, WS. |
臺北醫學大學 |
2013 |
In utero exposure to environmental lead and manganese and neurodevelopment at 2 years of age
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Lin, CC;Chen, YC;Su, FC;Lin, CM;Liao, HF;Hwang, YH;Hsieh, WS;Jeng, SF;Su, YN;Chen, PC |
國家衛生研究院 |
2012-10-10 |
Targeted disruption in mice of a Neural Stem Cell-Maintaining, KRAB-Zn finger-encoding gene that has rapidly evolved in the human lineage
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Chien, HC;Wang, HY;Su, YN;Lai, KY;Lu, LC;Chen, PC;Tsai, SF;Wu, CI;Hsieh, WS;Shen, CKJ |
國立臺北護理健康大學 |
2011 |
Favorable neonatal outcomes among live births to marriage immigrant mothers: evidence of healthy immigrant mother effect from Taiwan.
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張蓓貞; Hsieh, WS;Hsieh, CJ;Jeng, SF;Liao, HF;Su, YN;Lin, SJ;Chang, PJ;Chen, PC |
國立臺灣大學 |
2010 |
Phenotypic Analyses and Mutation Screening of the SLC26A4 and FOXI1 Genes in 101 Taiwanese Families with Bilateral Nonsyndromic Enlarged Vestibular Aqueduct (DFNB4) or Pendred Syndrome
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Wu, CC; Lu, YC; Chen, PJ; Yeh, PL; Su, YN; Hwu, WL; Hsu, CJ |
國立臺灣大學 |
2010 |
Pre-implantation genetic diagnosis (Embryo Screening) for enlarged vestibular aqueduct due to SLC26A4 mutation
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Wu, CC; Lin, SY; Su, YN; Fang, MY; Chen, SU; Hsu, CJ |
國立臺灣大學 |
2009-03 |
Association of novel chymotrypsin C (CTRC) gene variations and haplotypes in patients with chronic pancreatitis in Chinese in Taiwan
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Chang, MC; Chang, YT; Wei, SC; Liang, PC; Jan, IS; Su, YN; Kuo, CH; Wong, JM |
國立臺灣大學 |
2009 |
Neonatal and pregnancy outcome in primary antiphospholipid syndrome: A 10-year experience in one medical center.
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Chou, AK; Hsieh, SC; Su, YN; Jeng, SF; Chen, CY; Chou, HC; Tsao, PN; Hsieh, WS. |
國立臺灣大學 |
2008-12 |
PGD of beta-thalassaemia and HLA haplotypes using OmniPlex whole genome amplification
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Chen, SU; Su, YN; Fang, MY; Chang, LJ; Tsai, YY; Lin, LT; Lee, CN; Yang, YS. |
國立臺灣大學 |
2008-11 |
Lipoprotein Lipase Mutation S447X Associated With Pancreatic Calcification and Steatorrhea in Hyperlipidemic Pancreatitis.
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Chang, YT; Chang, MC; Su, TC; Liang, PC; Su, YN; Kuo, CH; Wei, SC; Wong, JM. |
國立臺灣大學 |
2008-11 |
PGD of beta-thalassaemia and HLA haplotypes using OmniPlex whole genome amplification.
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Chen, SU; Su, YN; Fang, MY; Chang, LJ; Tsai, YY; Lin, LT; Lee, CN; Yang, YS. |
國立臺灣大學 |
2008-11 |
’Big-eyed frog’ sign on spatiotemporal image correlation (STIC) in the antenatal diagnosis of transposition of the great arteries
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Shih, JC; Shyu, MK; Su, YN; Chiang, YC; Lin, CH; Lee, CN |
國立臺灣大學 |
2008-10 |
PHOX2B Mutation-Confirmed Congenital Central Hypoventilation Syndrome in a Chinese Family.
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Lee, P; Su, YN; Yu, CJ; Yang, PC; Wu, HD |
國家衛生研究院 |
2008-09 |
CYP1A1 Ile462Val and GSTT1 modify the effect of cord blood cotinine on neurodevelopment at 2 years of age
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Hsieh, CJ;Liao, HF;Wu, KY;Hsieh, WS;Su, YN;Jeng, SF;Yu, SN;Chen, PC |
國立臺灣大學 |
2008-09 |
CYP1A1 Ile462Val and GSTT1 modify the effect of cord blood cotinine on neurodevelopment at two years of age
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Hsieh, CJ; Liao, HF; Wu, KY; Hsieh, WS; Su, YN; Jeng, SF; Yu, SN; Chen, PC |
國立臺灣大學 |
2008-08 |
Comparison of the mismatch-specific endonuclease method and denaturing high-performance liquid chromatography for the identification of HBB gene mutations
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Hung, CC; Su, YN; Lin, CY; Chang, YF; Chang, CH; Cheng, WF; Chen, CA; Lee, CN; Lin, WL |
國立臺灣大學 |
2008-07 |
Connective tissue growth factor linked to the E7 tumor antigen generates potent antitumor immune responses mediated by an antiapoptotic mechanism.
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Cheng, WF; Chang, MC; Sun, WZ; Lee, CN; Lin, HW; Su, YN; Hsieh, CY; Chen, CA |
國立臺灣大學 |
2008-06 |
Mutation spectrum of 122 hemophilia A families from Taiwanese population by LD-PCR, DHPLC, multiplex PCR and evaluating the clinical application of HRM
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Lin, SY; Su, YN; Hung, CC; Tsay, W; Chiou, SS; Chang, CT; Ho, HN; Lee, CN |
國立臺灣大學 |
2008-05 |
Macular amyloidosis presenting in an incontinentia pigmenti-like pattern with subepidermal blister formation
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Wu, JJ; Su, YN; Hsiao, CH; Jee, SH; Tjiu, JW; Chen, JS. |
國立臺灣大學 |
2008-04 |
High perinatal seroprevalence of cytomegalovirus in northern Taiwan
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Chen, MH; Chen, PC; Jeng, SF; Hsieh, CJ; Su, FC; Liao, HF; Su, YN; Lin, SJ; Hsieh, WS |
國立臺灣大學 |
2008-02 |
Identification of deletion and duplication genotypes of the PMP22 gene using PCR-RFLP, competitive multiplex PCR, and multiplex ligation-dependent probe amplification: A comparison
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Hung, CC; Lee, CN; Lin, CY; Cheng, WF; Chen, CA; Hsieh, ST; Yang, CC; Jong, YJ; Su, YN; Lin, WL |
國立臺灣大學 |
2008-02 |
Genotyping of the G1138A mutation of the FGFR3 gene in patients with achondroplasia using high-resolution melting analysis.
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Hung, CC; Lee, CN; Chang, CH; Jong, YJ; Chen, CP; Hsieh, WS; Su, YN; Lin, WL. |
中國醫藥大學 |
2008-02 |
Corrections to the LDLR gene polymorphisms identified in a Taiwanese population.
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(Yang KC); (Su YN); (Shew JY); (Yang KY); (Tseng WK); (Wu CC)*; 李源德(Yuan-Teh, Lee) |
國立臺灣大學 |
2008-01 |
Association of cystic fibrosis transmembrane conductance regulator (CFTR) mutation/variant/haplotype and TNF- promoter polymorphism in hyperlipidemic pancreatitis
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Chang YT; Chang MC; Su TC; Liang PC; Su YN; Kuo CH; Wei SC; Wong JM |
國立臺灣大學 |
2008 |
Rapid prenatal diagnosis of spinal muscular atrophy by denaturing high-performance liquid chromatography system
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Shaw, SW; Cheng, PJ; Chang, SD; Lin, YT; Hung, CC; Chen, CP; Su, YN |
Showing items 1-25 of 114 (5 Page(s) Totally) 1 2 3 4 5 > >> View [10|25|50] records per page
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