作者
- Chen, C.P. (96)
- Chen, W.L. (23)
- Chen, Y.T. (37)
- Chern, S.R. (81)
- Lee, C.C. (28)
- Su, J.W. (37)
- Su, Y.N. (105)
- Tsai, F.J. (42)
- Wang, W. (94)
- Wu, P.C. (36)
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總筆數:105
| 篇名 | 作者 | 刊名 | 出版年 | 查看 |
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| Decreased maternal serum placenta growth factor in early second trimesterand preeclampsia |
Su, Y.N.;Lee, C.N.;Cheng, W.F.;Shau, W.Y.;Chow, S.N.;Hsieh, F.J.; |
Obstetrics and Gynecology |
2001-06-01 |
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| Current Aspects in the Molecular Genetics and Diagnostics of SpinalMuscular Atrophy |
Chien, S.C.;Su, Y.N.; |
Taiwanese Journal of Obstetrics and Gynecology |
2005-09-01 |
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| Septic Shock after Intracervical Laminaria Insertion |
Lin, S.Y.;Cheng, W.F.;Su, Y.N.;Chen, C.A.;Lee, C.N.; |
Taiwanese Journal of Obstetrics and Gynecology |
2006-03-01 |
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| Prenatal Magnetic Resonance Imaging, Ultrasound Imaging Findings andGenetic Analysis of Concomitant Rhabdomyomas and Cerebral Tuberous Sclerosis |
Chen, C.P.;Su, Y.N.;Chang, T.Y.;Liu, Y.P.;Tsai, F.J.;Hwang, J.K.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2009-09-01 |
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| 22q 11.2 Microdeletion in a Fetus With Double-outlet Right Ventricle,Pulmonary Stenosis and a Ventricular Septal Defect: Prenatal Diagnosis byArray Comparative Genomic Hybridization |
Chen, C.P.;Su, Y.N.;Chang, T.Y.;Chern, S.R.;Tsai, F.J.;Hwang, J.K.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2009-12-01 |
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| Terminal 2q Deletion and Distal 15q Duplication: Prenatal Diagnosis byArray Comparative Genomic Hybridization Using Uncultured Amniocytes |
Chen, C.P.;Su, Y.N.;Tsai, F.J.;Lin, H.H.;Chern, S.R.;Lee, M.S.;Hwang, J.K.;Chen, T.H.T.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2009-12-01 |
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| 22q 11.2 Microdeletion in a Fetus With Double-outlet Right Ventricle,Pulmonary Stenosis and a Ventricular Septal Defect: Prenatal Diagnosis byArray Comparative Genomic Hybridization |
Chen, C.P.;Su, Y.N.;Chang, T.Y.;Chern, S.R.;Tsai, F.J.;Hwang, J.K.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2009-12-01 |
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| Terminal 2q Deletion and Distal 15q Duplication: Prenatal Diagnosis byArray Comparative Genomic Hybridization Using Uncultured Amniocytes |
Chen, C.P.;Su, Y.N.;Tsai, F.J.;Lin, H.H.;Chern, S.R.;Lee, M.S.;Hwang, J.K.;Chen, T.H.T.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2009-12-01 |
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| Prenatal Diagnosis of a 4.9-Mb Deletion of 10q11.21 @? q11.23 by ArrayComparative Genomic Hybridization |
Chen, C.P.;Su, Y.N.;Chern, S.R.;Tsai, F.J.;Hsu, C.Y.;Lee, C.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-03-01 |
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| Rapid Genome-wide Aneuploidy Diagnosis Using Uncultured Amniocytes andArray Comparative Genomic Hybridization in Pregnancy With AbnormalUltrasound Findings Detected in Late Second and Third Trimesters |
Chen, C.P.;Su, Y.N.;Tsai, F.J.;Chern, S.R.;Hsu, C.Y.;Huang, M.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-03-01 |
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| Abnormally Flat Facial Profile on Two- and Three-dimensional Ultrasoundand Array Comparative Genomic Hybridization for the Diagnosis ofPallister-Killian Syndrome |
Chen, C.P.;Su, Y.N.;Hsu, C.Y.;Tsai, F.J.;Chien, S.C.;Chern, S.R.;Lee, M.S.;Wu, P.C.;Chen, H.E.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-03-01 |
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| Second-trimester Maternal Serum Quadruple Test for Down SyndromeScreening: A Taiwanese Population-based Study |
Shaw, S.W.S.;Lin, S.Y.;Lin, C.H.;Su, Y.N.;Cheng, P.J.;Lee, C.N.;Chen, C.P.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-03-01 |
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| Prenatal Diagnosis of a 4.9-Mb Deletion of 10q11.21 @? q11.23 by ArrayComparative Genomic Hybridization |
Chen, C.P.;Su, Y.N.;Chern, S.R.;Tsai, F.J.;Hsu, C.Y.;Lee, C.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-03-01 |
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| Rapid Genome-wide Aneuploidy Diagnosis Using Uncultured Amniocytes andArray Comparative Genomic Hybridization in Pregnancy With AbnormalUltrasound Findings Detected in Late Second and Third Trimesters |
Chen, C.P.;Su, Y.N.;Tsai, F.J.;Chern, S.R.;Hsu, C.Y.;Huang, M.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-03-01 |
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| Abnormally Flat Facial Profile on Two- and Three-dimensional Ultrasoundand Array Comparative Genomic Hybridization for the Diagnosis ofPallister-Killian Syndrome |
Chen, C.P.;Su, Y.N.;Hsu, C.Y.;Tsai, F.J.;Chien, S.C.;Chern, S.R.;Lee, M.S.;Wu, P.C.;Chen, H.E.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-03-01 |
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| Second-trimester Molecular Prenatal Diagnosis of Sporadic ApertSyndrome Following Sonographic Findings of Mild Ventriculomegaly andClenched Hands Mimicking Trisomy 18 |
Chen, C.P.;Su, Y.N.;Hsu, C.Y.;Ling, P.Y.;Tsai, F.J.;Chern, S.R.;Wu, P.C.;Chen, H.E.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-03-01 |
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| Second-trimester Maternal Serum Quadruple Test for Down SyndromeScreening: A Taiwanese Population-based Study |
Shaw, S.W.S.;Lin, S.Y.;Lin, C.H.;Su, Y.N.;Cheng, P.J.;Lee, C.N.;Chen, C.P.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-03-01 |
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| Apert Syndrome Associated With Upper Airway Obstruction andGastroesophageal Reflux Inducing Polyhydramnios in the Third Trimester |
Chen, C.P.;Lin, S.P.;Su, Y.N.;Chen, C.Y.;Tsai, F.J.;Liu, Y.P.;Chern, S.R.;Wu, P.C.;Chen, H.E.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-06-01 |
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| Mosaic Tetrasomy 12P With Discrepancy Between Fetal Tissues andExtraembryonic Tissues: Molecular Analysis and Possible Mechanism ofFormation |
Chen, C.P.;Su, Y.N.;Chern, S.R.;Tsai, F.J.;Wu, P.C.;Chen, H.E.C.;Chiang, S.S.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-06-01 |
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| Prenatal Diagnosis and Molecular Cytogenetic Characterization of aSmall Supernumerary Marker Chromosome Derived from Chromosome 18 andAssociated With a Reciprocal Translocation Involving Chromosomes 17 And 18 |
Chen, C.P.;Lin, C.C.;Su, Y.N.;Tsai, F.J.;Chen, J.T.;Chern, S.R.;Lee, C.C.;Town, D.D.;Chen, L.F.;Wu, P.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-06-01 |
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| Detection and Comparison of Cytomegalovirus DNA Levels in AmnioticFluid and Fetal Ascites in a Second-Trimester Fetus With Massive Ascites,Hyperechogenic Bowel, Ventriculomegaly and Intrauterine Growth Restriction |
Chen, C.P.;Su, Y.N.;Chern, S.R.;Wang, T.Y.;Tsai, F.J.;Lin, H.H.;Wu, P.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-06-01 |
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| Fetal Magnetic Resonance Imaging Demonstration Of Central NervousSystem Abnormalities and Polydactyly Associated With Joubert Syndrome |
Chen, C.P.;Su, Y.N.;Huang, J.K.;Liu, Y.P.;Tsai, F.J.;Yang, C.K.;Huang, J.P.;Chen, C.Y.;Wu, P.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-06-01 |
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| Prenatal Diagnosis and Molecular Cytogenetic Characterization of DeNovo Partial Trisomy 7p (7p15.3->pter) and Partial Monosomy 13q(13q33.3->qter) Associated With Dandy-Walker Malformation, Abnormal SkullDevelopment and Microcephaly |
Chen, C.P.;Chen, M.;Su, Y.N.;Tsai, F.J.;Chern, S.R.;Hsu, C.Y.;Wu, P.C.;Town, D.D.;Lee, D.J.;Ma, G.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-09-01 |
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| Mosaic Ring Chromosome 18, Ring Chromosome 18 Duplication/Deletion andDisomy 18: Perinatal Findings and Molecular Cytogenetic Characterization byFluorescence In Situ Hybridization and Array Comparative GenomicHybridization |
Chen, C.P.;Kuo, Y.T.;Lin, S.P.;Su, Y.N.;Chen, Y.J.;Hsueh, R.Y.;Lin, Y.H.;Wu, P.C.;Lee, C.C.;Chen, Y.T.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-09-01 |
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| Mosaic Trisomy 7 at Amniocentesis: Prenatal Diagnosis and MolecularGenetic Analyses |
Chen, C.P.;Su, Y.N.;Chern, S.R.;Hwu, Y.M.;Lin, S.P.;Hsu, C.H.;Tsai, F.J.;Wang, T.Y.;Wu, P.C.;Lee, C.C.;Chen, Y.T.;Chen, L.F.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-09-01 |
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| Mosaic Trisomy 9 at Amniocentesis: Prenatal Diagnosis and MolecularGenetic Analyses |
Chen, C.P.;Lin, H.M.;Su, Y.N.;Chern, S.R.;Tsai, F.J.;Wu, P.C.;Lee, C.C.;Chen, Y.T.;Lee, M.S.;Pan, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-09-01 |
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| Prenatal Diagnosis and Molecular Cytogenetic Characterization of aSmall Supernumerary Marker Chromosome Derived From Chromosome 22 |
Chen, C.P.;Lin, C.C.;Su, Y.N.;Tsai, F.J.;Chern, S.R.;Lee, C.C.;Chen, W.L.;Chen, L.F.;Wu, P.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-09-01 |
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| Prenatal Diagnosis of Rhabdomyomas and Cerebral Tuberous Sclerosis byMagnetic Resonance Imaging in One Fetus of a Dizygotic Twin PregnancyAssociated With a Frameshift Mutation in the TSC2 Gene |
Chen, C.P.;Su, Y.N.;Chang, T.Y.;Liu, Y.P.;Tsai, F.J.;Chen, M.R.;Hwang, J.K.;Chen, T.H.T.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-09-01 |
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| Balanced Reciprocal Translocations Detected at Amniocentesis |
Chen, C.P.;Wu, P.C.;Lin, C.J.;Su, Y.N.;Chern, S.R.;Tsai, F.J.;Lee, C.C.;Town, D.D.;Chen, W.L.;Chen, L.F.;Lee, M.S.;Pan, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-12-01 |
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| Chromosome 1p36 Deletion Syndrome: Prenatal Diagnosis, MolecularCytogenetic Characterization and Fetal Ultrasound Findings |
Chen, C.P.;Chen, M.;Su, Y.N.;Hsu, C.Y.;Tsai, F.J.;Chern, S.R.;Wu, P.C.;Lee, C.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-12-01 |
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| Ellis-Van Creveld Syndrome: Prenatal Diagnosis, Molecular Analysis andGenetic Counseling |
Chen, C.P.;Su, Y.N.;Hsu, C.Y.;Chern, S.R.;Tsai, F.J.;Wu, P.C.;Chen, P.T.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-12-01 |
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| Partial Trisomy 16p (16p12.2->pter) and Partial Monosomy 22q (22q13.31->qter) Presenting With Fetal Ascites and Ventriculomegaly: PrenatalDiagnosis and Array Comparative Genomic Hybridization Characterization |
Chen, C.P.;Su, Y.N.;Young, R.S.H.;Tsai, F.J.;Wu, P.C.;Chern, S.R.;Town, D.D.;Pan, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-12-01 |
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| Partial Trisomy 10q (10q25.1 ->qter) and Partial Monosomy 13q(13q34->qter) Presenting With Fetal Pyelectasis: Prenatal Diagnosis andArray Comparative Genomic Hybridization Characterization |
Chen, C.P.;Su, Y.N.;Tsai, F.J.;Chern, S.R.;Hsu, C.Y.;Wu, P.C.;Lee, C.C.;Chen, W.L.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-12-01 |
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| Recurrent Distal 16q Duplication and Terminal 22q Deletion: PrenatalDiagnosis and Genetic Counseling |
Chen, C.P.;Huang, M.C.;Su, Y.N.;Tsai, F.J.;Wu, P.C.;Lee, C.C.;Town, D.D.;Pan, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2010-12-01 |
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| Inv dup del(9p): Prenatal diagnosis and molecular cytogeneticcharacterization by fluorescence in situ hybridization and arraycomparative genomic hybridization |
Chen, C.P.;Su, Y.N.;Chern, S.R.;Hsu, C.Y.;Tsai, F.J.;Wu, P.C.;Lee, C.C.;Chen, Y.T.;Lee, M.S.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-03-01 |
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| Rapid aneuploidy diagnosis by multiplex ligation-dependent probeamplification and array comparative genomic hybridization in pregnancy withmajor congenital malformations |
Chen, C.P.;Su, Y.N.;Lin, S.Y.;Chang, C.L.;Wang, Y.L.;Huang, J.P.;Chen, C.Y.;Hung, F.Y.;Chen, Y.Y.;Wu, P.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-03-01 |
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| Successful application of the strategy of blastocyst biopsy,vitrification, whole genome amplification, and thawed embryo transfer forpreimplantation 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.;Chen, S.U.;Yang, Y.S.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-03-01 |
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| Prenatal diagnosis and molecular cytogenetic characterization of aderivative chromosomeder(18;18)(q10;q10)del(18)(q11.1q12.1)del(18)(q22.1q22.3) presenting asapparent isochromosome 18q in a fetus with holoprosencephaly |
Chen, C.P.;Kuo, Y.K.;Su, Y.N.;Chern, S.R.;Tsai, F.J.;Wu, P.C.;Chen, Y.T.;Town, D.D.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-06-01 |
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| Prenatal diagnosis and molecular cytogenetic characterization ofmosaicism for a small supernumerary marker chromosome derived from ringchromosome 4 |
Chen, C.P.;Chen, M.;Su, Y.N.;Tsai, F.J.;Chern, S.R.;Wu, P.C.;Chen, W.L.;Chen, L.F.;Pan, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-06-01 |
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| Cytogenetic discrepancy between uncultured amniocytes and culturedamniocytes in mosaic isochromosome 20q detected at amniocentesis |
Chen, C.P.;Liou, J.D.;Chiang, C.H.;Su, Y.N.;Chern, S.R.;Tsai, F.J.;Wu, P.C.;Chen, Y.T.;Lee, C.C.;Chen, W.L.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-06-01 |
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| Prenatal diagnosis and array comparative genomic hybridizationcharacterization of a de novo interstitial deletion of chromosome 20p |
Chen, C.P.;Su, Y.N.;Chern, S.R.;Tsai, F.J.;Wu, P.C.;Lee, C.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-06-01 |
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| Partial monosomy 13q (13q21.32->qter) and partial trisomy 8p(8p12->pter) presenting with anencephaly and increased nuchal translucency:array comparative genomic hybridization characterization |
Chen, C.P.;Su, Y.N.;Tsai, F.J.;Lin, M.H.;Wu, P.C.;Chern, S.R.;Lee, C.C.;Pan, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-06-01 |
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| Prenatal diagnosis of mosaic trisomy 8: Clinical report and literaturereview |
Chen, C.P.;Chen, M.;Pan, Y.J.;Su, Y.N.;Chern, S.R.;Tsai, F.J.;Chen, Y.T.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-09-01 |
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| De novo duplication of Xq22.1->q24 with a disruption of the NXF genecluster in a mentally retarded woman with short stature and prematureovarian failure |
Chen, C.P.;Su, Y.N.;Lin, H.H.;Chern, S.R.;Tsai, F.J.;Wu, P.C.;Lee, C.C.;Chen, Y.T.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-09-01 |
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| Chromosome 1p32-p31 deletion syndrome: Prenatal diagnosis by arraycomparative genomic hybridization using uncultured amniocytes andassociation with NFIA haploinsufficiency, ventriculomegaly, corpus callosumhypogenesis, abnormal external genitalia, and intrauterine growthrestriction |
Chen, C.P.;Su, Y.N.;Chen, Y.Y.;Chern, S.R.;Liu, Y.P.;Wu, P.C.;Lee, C.C.;Chen, Y.T.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-09-01 |
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| Chromosome 15q overgrowth syndrome: Prenatal diagnosis, molecularcytogenetic characterization, and perinatal findings in a fetus withdup(15)(q26.2q26.3) |
Chen, C.P.;Lin, Y.H.;Au, H.K.;Su, Y.N.;Hsu, C.Y.;Liu, Y.P.;Wu, P.C.;Chern, S.R.;Chen, Y.T.;Chen, L.F.;Hsieh, A.H.M.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-09-01 |
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| Prenatal diagnosis of mosaic trisomy 2: Discrepancy between molecularcytogenetic analyses of uncultured amniocytes and karyotyping of culturedamniocytes in a pregnancy with severe fetal intrauterine growth restriction |
Chen, C.P.;Su, Y.N.;Lin, S.Y.;Chern, S.R.;Chen, Y.T.;Lee, M.S.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-09-01 |
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| Prenatal diagnosis and molecular cytogenetic characterization of amosaic derivative Y chromosome derived from a de novo unbalanced reciprocalYq;13q translocation |
Chen, C.P.;Su, Y.N.;Chen, M.;Huang, J.P.;Tsai, F.J.;Wu, P.C.;Chen, W.L.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-09-01 |
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| Prenatal diagnosis of microvillus inclusion disease |
Chen, C.P.;Su, Y.N.;Chern, S.R.;Wu, P.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-09-01 |
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| Prenatal diagnosis of directly transmitted benign 4q12-q13.1quadruplication associated with tandem segmental amplifications of theLPHN3 gene |
Chen, C.P.;Su, Y.N.;Chen, Y.T.;Chen, W.L.;Hsu, L.J.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-09-01 |
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| Mosaic deletion-duplication syndrome of chromosome 3: Prenatalmolecular cytogenetic diagnosis using cultured and uncultured amniocytesand association with fetoplacental discrepancy |
Chen, C.P.;Su, Y.N.;Hsu, C.Y.;Chern, S.R.;Lee, C.C.;Chen, Y.T.;Chen, W.L.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-12-01 |
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| A de novo duplication of chromosome 21q22.11->qter associated with Downsyndrome: Prenatal diagnosis, molecular cytogenetic characterization andfetal ultrasound findings |
Chen, C.P.;Huang, H.K.;Ling, P.Y.;Su, Y.N.;Chen, M.;Tsai, F.J.;Wu, P.C.;Chern, S.R.;Chen, Y.T.;Lee, C.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-12-01 |
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