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	2020-02-12T04:06:04Z	Identification of fibrillin-1 gene mutations in Marfan syndrome by high-resolution melting analysis	Su Y.-N.;Niu D.-M;Ho H.-N;Cheng W.-F;Lin S.-P;Yu C.-C;Chiu H.-H;Chang C.-H;Lin C.-Y;Cheng H.-Y;CHIEN-NAN LEE;Lin S.-Y;Hung C.-C; Hung C.-C; Lin S.-Y; CHIEN-NAN LEE; Cheng H.-Y; Lin C.-Y; Chang C.-H; Chiu H.-H; Yu C.-C; Lin S.-P; Cheng W.-F; Ho H.-N; Niu D.-M; Su Y.-N.
臺大學術典藏	2020-02-12T04:06:04Z	Identification of CpG methylation of the SNRPN gene by methylation-specific multiplex PCR	Lin S.-P; Niu D.-M; Lee N.-C; Cheng W.-F; Chen C.-P; Lin W.-L; CHIEN-NAN LEE; Su Y.-N.; Su Y.-N.;CHIEN-NAN LEE;Lin W.-L;Chen C.-P;Cheng W.-F;Lee N.-C;Niu D.-M;Lin S.-P;Lin S.-Y;Hung C.-C; Hung C.-C; Lin S.-Y
臺大學術典藏	2020-02-12T04:06:04Z	Role of three-dimensional power Doppler in the antenatal diagnosis of placenta accreta: Comparison with gray-scale and color Doppler techniques	CHIEN-NAN LEE;Lin S.Y;Lin C.H;Shyu M.K;Su Y.N;Jaraquemada J.M.P;Shih J.C; Shih J.C; Jaraquemada J.M.P; Su Y.N; Shyu M.K; Lin C.H; Lin S.Y; CHIEN-NAN LEE
臺大學術典藏	2020-02-12T04:06:03Z	Second-trimester Maternal Serum Quadruple Test for Down Syndrome Screening: A Taiwanese Population-based Study	Chen C.-P.;CHIEN-NAN LEE;Cheng P.-J;Su Y.-N;Lin C.-H;Lin S.-Y;Shaw S.W.S; Shaw S.W.S; Lin S.-Y; Lin C.-H; Su Y.-N; Cheng P.-J; CHIEN-NAN LEE; Chen C.-P.
臺大學術典藏	2020-02-12T04:06:03Z	Mesothelin inhibits paclitaxel-induced apoptosis through the PI3K pathway	Cheng W.-F.; Hu Y.-H; Su Y.-N; CHIEN-NAN LEE; Hsieh C.-Y; Chang M.-C; Chen C.-A; Cheng W.-F.;Hu Y.-H;Su Y.-N;CHIEN-NAN LEE;Hsieh C.-Y;Chen C.-A;Chang M.-C
臺大學術典藏	2020-02-12T04:06:02Z	Preimplantation genetic diagnosis of �]-thalassemia using real-time polymerase chain reaction with fluorescence resonance energy transfer hybridization probes	Su Y.-N.;CHIEN-NAN LEE;Yang Y.-S;Lin L.-T;Tsai Y.-Y;Chang L.-J;Fang M.-Y;Lin S.-Y;Chen S.-U;Hung C.-C; Hung C.-C; Chen S.-U; Lin S.-Y; Fang M.-Y; Chang L.-J; Tsai Y.-Y; Lin L.-T; Yang Y.-S; CHIEN-NAN LEE; Su Y.-N.
臺大學術典藏	2020-02-12T04:06:00Z	Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome	Ho H.-N.;Su Y.-N;Lin C.-Y;Kuo P.-W;Tu M.-P;Fang M.-Y;Chen L.-Y;Hsu W.-M;Niu D.-M;Tung Y.-C;Hsieh W.-S;Li N.-C;Lin S.-P;Tsai W.-Y;Hung C.-C;CHIEN-NAN LEE;Lin S.-Y; Lin S.-Y; CHIEN-NAN LEE; Hung C.-C; Tsai W.-Y; Lin S.-P; Li N.-C; Hsieh W.-S; Tung Y.-C; 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	2020-02-12T04:05:59Z	Successful application of the strategy of blastocyst biopsy, vitrification, whole genome amplification, and thawed embryo transfer for preimplantation genetic diagnosis of neurofibromatosis type 1	Yang Y.-S.;Chen S.-U;Su Y.-N;CHIEN-NAN LEE;Chang L.-J;Tsai Y.-Y;Fang M.-Y;Lin S.-Y;Hung C.-C;Chen Y.-L; Chen Y.-L; Hung C.-C; Lin S.-Y; Fang M.-Y; Tsai Y.-Y; Chang L.-J; CHIEN-NAN LEE; Su Y.-N; Chen S.-U; Yang Y.-S.
臺大學術典藏	2020-02-12T04:05:59Z	Quantitative and qualitative analyses of the SNRPN gene using real-time PCR with melting curve analysis	Su Y.-N.;CHIEN-NAN LEE;Chen L.-Y;Chen C.-P;Lin S.-P;Lin S.-Y;Hung C.-C; Hung C.-C; Lin S.-Y; Lin S.-P; Chen C.-P; Chen L.-Y; CHIEN-NAN LEE; Su Y.-N.
臺大學術典藏	2020-02-12T04:05:58Z	Low penetrance of retinoblastoma for p.V654L mutation of the RB1 gene	Su Y.-N.; Chiou S.-S; Chao M.-C; Su Y.-N.;Chiou S.-S;Chao M.-C;Lin S.-P;Chen C.-P;CHIEN-NAN LEE;Lin S.-Y;Hung C.-C; Hung C.-C; Lin S.-Y; CHIEN-NAN LEE; Chen C.-P; Lin S.-P
臺大學術典藏	2020-02-12T04:05:58Z	Carrier screening for spinal muscular atrophy (SMA) in 107,611 pregnant women during the period 2005-2009: A prospective population-based cohort study	CHIEN-NAN LEE;Ho H.-N;Li H;Yang C.-C;Chang T.-S;Tsai C;Chern J.P.S;Chen F.-Y;Lin S.-Y;Hung C.-C;Su Y.-N; Su Y.-N; Hung C.-C; Lin S.-Y; Chen F.-Y; Chern J.P.S; Tsai C; Chang T.-S; Yang C.-C; Li H; Ho H.-N; CHIEN-NAN LEE
臺大學術典藏	2020-02-12T04:05:57Z	Newborn genetic screening for hearing impairment: A preliminary study at a tertiary center	Hsu C.-J.;Su Y.-N;CHIEN-NAN LEE;Tsao P.-N;Hsieh W.-S;Lin S.-Y;Hung C.-C;Wu C.-C; Wu C.-C; Hung C.-C; Lin S.-Y; Hsieh W.-S; Tsao P.-N; CHIEN-NAN LEE; Su Y.-N; Hsu C.-J.
臺大學術典藏	2020-02-12T04:05:57Z	Two cases of Lowe syndrome presenting as increased fetal nuchal translucency	Su Y.-N.;Lin C.-H;Shih J.-C;CHIEN-NAN LEE;Lin S.-Y; Lin S.-Y; CHIEN-NAN LEE; Shih J.-C; Lin C.-H; Su Y.-N.
臺大學術典藏	2020-02-12T04:05:56Z	A whole genome methylation analysis of systemic lupus erythematosus: Hypomethylation of the IL10 and IL1R2 promoters is associated with disease activity	Ho H.-N.;Su Y.-N;Niu D.-M;Hsieh W.S;Chen L.-Y;Hung C.-C;Chen P.-C;Chuang E.Y;Lai L.-C;Tsai M.-H;CHIEN-NAN LEE;Lin Y.-C;Hsieh S.-C;Lin S.-Y; Lin S.-Y; Hsieh S.-C; Lin Y.-C; CHIEN-NAN LEE; 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	2020-02-12T04:05:56Z	Prenatal diagnosis of a fetus with a de novo trisomy 12p by array-comparative genomic hybridization (array-CGH)	Su Y.-N.;CHIEN-NAN LEE;Shin J.-C;Lin S.-Y;Lin C.-H;Hung C.-C; Hung C.-C; Lin C.-H; Lin S.-Y; Shin J.-C; CHIEN-NAN LEE; Su Y.-N.
臺大學術典藏	2020-02-12T04:05:56Z	Diagnosis of Transposition of the Great Arteries in the Fetus	CHIEN-NAN LEE;Shyu M.-K;Wu E.-T;Lin S.-Y;Su Y.-N;Lin T.-H;Lin C.-H;Huang S.-C;Shih J.-C; Shih J.-C; Huang S.-C; Lin C.-H; Lin T.-H; Su Y.-N; Lin S.-Y; Wu E.-T; Shyu M.-K; CHIEN-NAN LEE
臺大學術典藏	2020-02-12T04:05:55Z	Re: Microarray application in prenatal diagnosis: A position statement from the cytogenetics working group of the Italian Society of Human Genetics (SIGU), November 2011	Su Y.-N.;Lin T.-H;Shih J.-C;Lin C.-H;Lin S.-Y;CHIEN-NAN LEE; CHIEN-NAN LEE; Lin S.-Y; Lin C.-H; Shih J.-C; Lin T.-H; Su Y.-N.
臺大學術典藏	2020-02-12T04:05:55Z	Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: A cohort study of 3171 pregnancies	Su Y.-N.;Lin T.-H;Shih J.-C;Lin C.-H;Lin S.-Y;CHIEN-NAN LEE; CHIEN-NAN LEE; Lin S.-Y; Lin C.-H; Shih J.-C; Lin T.-H; Su Y.-N.
臺大學術典藏	2020-02-12T04:05:54Z	Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: A cohort study of 3171 pregnancies: Editorial comment	Su Y.-N.; Lin T.-H; Shih J.-C; Lin C.-H; Su Y.-N.;Lin T.-H;Shih J.-C;Lin C.-H;Lin S.-Y;CHIEN-NAN LEE; CHIEN-NAN LEE; Lin S.-Y
臺大學術典藏	2020-02-12T04:05:54Z	Should array CGH be applied to all routine prenatal care?	Su Y.N.;Chung C.H;Shih J.C;CHIEN-NAN LEE;Lin S.Y;Lin T.H; Lin T.H; Lin S.Y; CHIEN-NAN LEE; Shih J.C; Chung C.H; Su Y.N.
臺大學術典藏	2020-02-12T04:05:54Z	Intraperitoneal and intracardiac transfusion of recurrent fetal erythroblastosis due to anti-M alloimmunization with unfavorable outcome	CHIEN-NAN LEE;Su Y.-N;Lin S.-Y;Lin C.-H;Shih J.-C;Lin T.-H; Lin T.-H; Shih J.-C; Lin C.-H; Lin S.-Y; Su Y.-N; CHIEN-NAN LEE
臺大學術典藏	2020-02-12T04:05:53Z	Clinical utility of array comparative genomic hybridisation for prenatal diagnosis: A cohort study of 3171 pregnancies	Su Y.-N.;Lin T.-H;Shih J.-C;Lin C.-H;Lin S.-Y;CHIEN-NAN LEE; CHIEN-NAN LEE; Lin S.-Y; Lin C.-H; Shih J.-C; Lin T.-H; Su Y.-N.
臺大學術典藏	2020-02-12T04:05:53Z	Maternal ascites after thoracoamniotic shunting	CHIEN-NAN LEE;Su Y.-N;Shih J.-C;Lin T.-H; Lin T.-H; Shih J.-C; Su Y.-N; CHIEN-NAN LEE
臺大學術典藏	2020-02-12T04:05:52Z	Authors' response to: The clinical utility and indications of chromosomal microarray analysis in prenatal diagnosis	Heard I.;Su Y.-N;Shih J.-C;Lin S.-Y;CHIEN-NAN LEE; CHIEN-NAN LEE; Lin S.-Y; Shih J.-C; Su Y.-N; Heard I.
臺大學術典藏	2020-02-12T04:05:52Z	Resolution of high uterine artery pulsatility index and notching following sildenafil citrate treatment in a growth-restricted pregnancy	CHIEN-NAN LEE;Hsu H.C;Shih J.C;Su Y.N;Lin T.H; Lin T.H; Su Y.N; Shih J.C; Hsu H.C; CHIEN-NAN LEE

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