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Showing items 516-540 of 715 (29 Page(s) Totally)
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Institution	Date	Title	Author
臺大學術典藏	2020-02-10T06:49:26Z	Preimplantation genetic diagnosis (embryo screening) for enlarged vestibular aqueduct due to SLC26A4 mutation	Wu C.-C;Shin-Yu Lin;Su Y.-N;Fang M.-Y;Chen S.-U;Hsu C.-J.; Wu C.-C; SHIN-YU LIN; Su Y.-N; Fang M.-Y; Chen S.-U; Hsu C.-J.
臺大學術典藏	2020-02-10T06:49:24Z	Rapid aneuploidy diagnosis by multiplex ligation-dependent probe amplification and array comparative genomic hybridization in pregnancy with major congenital malformations	Chen C.-P;Su Y.-N;Shin-Yu Lin;Chang C.-L;Wang Y.-L;Huang J.-P;Chen C.-Y;Hung F.-Y;Chen Y.-Y;Wu P.-C;Wang W.; Chen C.-P; Su Y.-N; SHIN-YU LIN; Chang C.-L; Wang Y.-L; Huang J.-P; Chen C.-Y; Hung F.-Y; Chen Y.-Y; Wu P.-C; Wang W.
臺大學術典藏	2020-02-10T06:49:24Z	Quantitative and qualitative analyses of the SNRPN gene using real-time PCR with melting curve analysis	Hung C.-C;Shin-Yu Lin;Lin S.-P;Chen C.-P;Chen L.-Y;Lee C.-N;Su Y.-N.; Hung C.-C; SHIN-YU LIN; Lin S.-P; Chen C.-P; Chen L.-Y; Lee C.-N; Su Y.-N.
臺大學術典藏	2020-02-10T06:49:24Z	Epigenetic profiling of the H19 differentially methylated region and comprehensive whole genome array-based analysis in Silver-Russell syndrome	Shin-Yu Lin;Lee C.-N;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.; SHIN-YU LIN; Lee C.-N; 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	2020-02-10T06:49:23Z	Carrier screening for spinal muscular atrophy (SMA) in 107,611 pregnant women during the period 2005-2009: A prospective population-based cohort study	Su Y.-N;Hung C.-C;Shin-Yu Lin;Chen F.-Y;Chern J.P.S;Tsai C;Chang T.-S;Yang C.-C;Li H;Ho H.-N;Lee C.-N.; Su Y.-N; Hung C.-C; SHIN-YU LIN; Chen F.-Y; Chern J.P.S; Tsai C; Chang T.-S; Yang C.-C; Li H; Ho H.-N; Lee C.-N.
臺大學術典藏	2020-02-10T06:49:23Z	Successful application of the strategy of blastocyst biopsy, vitrification, whole genome amplification, and thawed embryo transfer for preimplantation genetic diagnosis of neurofibromatosis type 1	Chen Y.-L;Hung C.-C;Shin-Yu Lin;Fang M.-Y;Tsai Y.-Y;Chang L.-J;Lee C.-N;Su Y.-N;Chen S.-U;Yang Y.-S.; Chen Y.-L; Hung C.-C; SHIN-YU LIN; Fang M.-Y; Tsai Y.-Y; Chang L.-J; Lee C.-N; Su Y.-N; Chen S.-U; Yang Y.-S.
臺大學術典藏	2020-02-10T06:49:22Z	Low penetrance of retinoblastoma for p.V654L mutation of the RB1 gene	Hung C.-C;Shin-Yu Lin;Lee C.-N;Chen C.-P;Lin S.-P;Chao M.-C;Chiou S.-S;Su Y.-N.; Hung C.-C; SHIN-YU LIN; Lee C.-N; Chen C.-P; Lin S.-P; Chao M.-C; Chiou S.-S; Su Y.-N.
臺大學術典藏	2020-02-10T06:49:21Z	Prenatal diagnosis of mosaic trisomy 2: Discrepancy between molecular cytogenetic analyses of uncultured amniocytes and karyotyping of cultured amniocytes in a pregnancy with severe fetal intrauterine growth restriction	Chen C.-P;Su Y.-N;Shin-Yu Lin;Chern S.-R;Chen Y.-T;Lee M.-S;Wang W.; Chen C.-P; Su Y.-N; SHIN-YU LIN; Chern S.-R; Chen Y.-T; Lee M.-S; Wang W.
臺大學術典藏	2020-02-10T06:49:21Z	Newborn genetic screening for hearing impairment: A preliminary study at a tertiary center	Wu C.-C;Hung C.-C;Shin-Yu Lin;Hsieh W.-S;Tsao P.-N;Lee C.-N;Su Y.-N;Hsu C.-J.; Wu C.-C; Hung C.-C; SHIN-YU LIN; Hsieh W.-S; Tsao P.-N; Lee C.-N; Su Y.-N; Hsu C.-J.
臺大學術典藏	2020-02-10T06:49:21Z	Two cases of Lowe syndrome presenting as increased fetal nuchal translucency	Shin-Yu Lin;Lee C.-N;Shih J.-C;Lin C.-H;Su Y.-N.; SHIN-YU LIN; Lee C.-N; Shih J.-C; Lin C.-H; Su Y.-N.
臺大學術典藏	2020-02-10T06:49:20Z	Genetic mutation in male patients with incontinentia pigmenti	Shin-Yu Lin;Tsao P.-N;Hsieh W.-S;Hung C.-C;Su Y.-N.; SHIN-YU LIN; Tsao P.-N; Hsieh W.-S; Hung C.-C; Su Y.-N.
臺大學術典藏	2020-02-10T06:49:13Z	Authors' response to: The clinical utility and indications of chromosomal microarray analysis in prenatal diagnosis	Lee C.-N;Shin-Yu Lin;Shih J.-C;Su Y.-N;Heard I.; Lee C.-N; SHIN-YU LIN; Shih J.-C; Su Y.-N; Heard I.
臺大學術典藏	2020-02-06T06:50:11Z	PGD of �]-thalassaemia and HLA haplotypes using OmniPlex whole genome amplification	Yang Y.-S.;Lee C.-N;Lin L.-T;Tsai Y.-Y;Chang L.-J;Fang M.-Y;Su Y.-N;SHEE-UAN CHEN; SHEE-UAN CHEN; Su Y.-N; Fang M.-Y; Chang L.-J; Tsai Y.-Y; Lin L.-T; Lee C.-N; Yang Y.-S.
臺大學術典藏	2020-02-06T06:50:06Z	Preimplantation genetic diagnosis of �]-thalassemia using real-time polymerase chain reaction with fluorescence resonance energy transfer hybridization probes	Hung C.-C;Shee-Uan Chen;Lin S.-Y;Fang M.-Y;Chang L.-J;Tsai Y.-Y;Lin L.-T;Yang Y.-S;Lee C.-N;Su Y.-N.; Hung C.-C; SHEE-UAN CHEN; Lin S.-Y; Fang M.-Y; Chang L.-J; Tsai Y.-Y; Lin L.-T; Yang Y.-S; Lee C.-N; Su Y.-N.
臺大學術典藏	2020-02-06T06:50:04Z	Preimplantation genetic diagnosis (embryo screening) for enlarged vestibular aqueduct due to SLC26A4 mutation	Wu C.-C;Lin S.-Y;Su Y.-N;Fang M.-Y;Shee-Uan Chen;Hsu C.-J.; Wu C.-C; Lin S.-Y; Su Y.-N; Fang M.-Y; SHEE-UAN CHEN; Hsu C.-J.
臺大學術典藏	2020-02-06T06:50:02Z	An update of preimplantation genetic diagnosis in gene diseases, chromosomal translocation, and aneuploidy screening	Chang L.-J;Shee-Uan Chen;Tsai Y.-Y;Hung C.-C;Fang M.-Y;Su Y.-N;Yang Y.-S.; Chang L.-J; SHEE-UAN CHEN; Tsai Y.-Y; Hung C.-C; Fang M.-Y; Su Y.-N; Yang Y.-S.
臺大學術典藏	2020-02-06T06:50:02Z	Successful application of the strategy of blastocyst biopsy, vitrification, whole genome amplification, and thawed embryo transfer for preimplantation genetic diagnosis of neurofibromatosis type 1	Chen Y.-L;Hung C.-C;Lin S.-Y;Fang M.-Y;Tsai Y.-Y;Chang L.-J;Lee C.-N;Su Y.-N;Shee-Uan Chen;Yang Y.-S.; Chen Y.-L; Hung C.-C; Lin S.-Y; Fang M.-Y; Tsai Y.-Y; Chang L.-J; Lee C.-N; Su Y.-N; SHEE-UAN CHEN; Yang Y.-S.
臺大學術典藏	2020-02-06T06:49:58Z	Blastocyst biopsy and vitrification are effective for preimplantation genetic diagnosis of monogenic diseases	Chang L.-J;Huang C.-C;Tsai Y.-Y;Hung C.-C;Fang M.-Y;Lin Y.-C;Su Y.-N;Shee-Uan Chen;Yang Y.-S.; Chang L.-J; Huang C.-C; Tsai Y.-Y; Hung C.-C; Fang M.-Y; Lin Y.-C; Su Y.-N; SHEE-UAN CHEN; Yang Y.-S.
臺大學術典藏	2020-02-06T06:49:57Z	Prenatal diagnosis of hypomethylation at KvDMR1 and Beckwith-Wiedemann syndrome in a pregnancy conceived byintracytoplasmic sperm injection and invitro fertilization andembryo transfer	Chen C.-P;Su Y.-N;Shee-Uan Chen;Chang T.-Y;Wu P.-C;Chern S.-R;Wu P.-S;Kuo Y.-L;Wang W.; Chen C.-P; Su Y.-N; SHEE-UAN CHEN; Chang T.-Y; Wu P.-C; Chern S.-R; Wu P.-S; Kuo Y.-L; Wang W.
臺大學術典藏	2020-02-06T06:49:57Z	A feasible strategy of preimplantation genetic diagnosis for carriers with chromosomal translocation: Using blastocyst biopsy and array comparative genomic hybridization	Huang C.-C;Chang L.-J;Tsai Y.-Y;Hung C.-C;Fang M.-Y;Su Y.-N;Chen H.-F;Shee-Uan Chen; Huang C.-C; Chang L.-J; Tsai Y.-Y; Hung C.-C; Fang M.-Y; Su Y.-N; Chen H.-F; SHEE-UAN CHEN
臺大學術典藏	2020-02-06T05:22:50Z	The possible use of colour flow Doppler in planning treatment in early invasive carcinoma of the cervix	Lee C.-N.; Chu J.-S.; Cheng S.-P.; Wei L.-H.; Su Y.-N.; Lee C.-N.;Chu J.-S.;Cheng S.-P.;Su Y.-N.;Wei L.-H.;WEN-FANG CHENG; WEN-FANG CHENG; Wei L.-H.; Su Y.-N.; Cheng S.-P.; Chu J.-S.; Lee C.-N.; WEN-FANG CHENG
臺大學術典藏	2020-02-06T05:22:49Z	Cervical pregnancy: Assessment with three-dimensional power Doppler imaging and successful management with selective uterine artery embolization	Hsieh F.-J.; Hsieh F.-J.;WEN-FANG CHENG;Lee C.-N.;Chiu W.-H.;Shih J.-C.;Su Y.-N.; Su Y.-N.; Shih J.-C.; Chiu W.-H.; Lee C.-N.; WEN-FANG CHENG; Hsieh F.-J.; Su Y.-N.; Shih J.-C.; Chiu W.-H.; Lee C.-N.; WEN-FANG CHENG
臺大學術典藏	2020-02-06T05:22:43Z	Decreased maternal serum placenta growth factor in early second trimester and preeclampsia	Hsieh F.J.;Chow S.N.;Shau W.Y.;WEN-FANG CHENG;Lee C.N.;Su Y.N.; Su Y.N.; Lee C.N.; WEN-FANG CHENG; Shau W.Y.; Chow S.N.; Hsieh F.J.; Su Y.N.; Lee C.N.; WEN-FANG CHENG; Shau W.Y.; Chow S.N.; Hsieh F.J.
臺大學術典藏	2020-02-06T05:22:39Z	Radical hysterectomy alone or combined with neoadjuvant chemotherapy in the treatment of early stage bulky cervical carcinoma	Hsieh C.-Y.;Su Y.-N.;Wei L.-H.;WEN-FANG CHENG;Chen C.-A.; Chen C.-A.; WEN-FANG CHENG; Wei L.-H.; Su Y.-N.; Hsieh C.-Y.; Chen C.-A.; WEN-FANG CHENG; Wei L.-H.; Su Y.-N.; Hsieh C.-Y.
臺大學術典藏	2020-02-06T05:22:38Z	Rapid detection of �]-globin gene (HBB) mutations coupling heteroduplex and primer-extension analysis by DHPLC	Hsieh F.-J.;Yu C.-L.;Tsao P.-N.;WEN-FANG CHENG;Chen C.-A.;Hung C.-C.;Lee C.-N.;Su Y.-N.; Su Y.-N.; Lee C.-N.; Hung C.-C.; Chen C.-A.; WEN-FANG CHENG; Tsao P.-N.; Yu C.-L.; Hsieh F.-J.; Su Y.-N.; Lee C.-N.; Hung C.-C.; Chen C.-A.; WEN-FANG CHENG; Tsao P.-N.; Yu C.-L.; Hsieh F.-J.

Showing items 516-540 of 715 (29 Page(s) Totally)
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