| 篇名 | 作者 | 刊名 | 出版年 | 查看 |
|---|
| The genetic implication for preceding generations of the prenatal diagnosisof interrupted aortic arch in association with unsuspected DiGeorge anomaly |
Puder, K.S.;Humes, R.A.;Gold, R.L.;Bawle, E.V.;Goyert, G.L.; |
American Journal of Obstetrics and Gynecology |
1995-07-01 |
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| Prenatal diagnosis of aneuploidy and deletion 22q11.2 in fetuses withultrasound detection of cardiac defects |
Moore, J.W.;Binder, G.A.;Berry, R.; |
American Journal of Obstetrics and Gynecology |
2004-12-01 |
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| Prenatal diagnosis of aneuploidy and deletion 22q11.2 in fetuses withultrasound detection of cardiac defects |
Moore, J.W.;Binder, G.A.;Berry, R.; |
American Journal of Obstetrics and Gynecology |
2004-12-01 |
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| Prenatal diagnosis of aneuploidy and deletion 22q11.2 in fetuses withultrasound detection of cardiac defects |
Moore, J.W.;Binder, G.A.;Berry, R.; |
American Journal of Obstetrics and Gynecology |
2004-12-01 |
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| Prospective study of 22q11 deletion analysis in fetuses with excessnuchal translucency |
Donnenfeld, A.E.;Cutillo, D.;Horwitz, J.;Knops, J.; |
American Journal of Obstetrics and Gynecology |
2006-02-01 |
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| Prospective study of 22q11 deletion analysis in fetuses with excessnuchal translucency |
Donnenfeld, A.E.;Cutillo, D.;Horwitz, J.;Knops, J.; |
American Journal of Obstetrics and Gynecology |
2006-02-01 |
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| Prenatal Diagnosis of Monosomy 17p (17p 13.3 @? pter) Associated WithPolyhydramnios, Intrauterine Growth Restriction, Ventriculomegaly, andMiller-Dieker Lissencephaly Syndrome in a Fetus |
Lin, C.Y.;Chen, C.P.;Liau, C.L.;Su, P.H.;Tsao, T.F.;Chang, T.Y.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2009-12-01 |
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| Prenatal Diagnosis of Monosomy 17p (17p 13.3 -> pter) Associated WithPolyhydramnios, Intrauterine Growth Restriction, Ventriculomegaly, andMiller-Dieker Lissencephaly Syndrome in a Fetus |
Lin, C.Y.;Chen, C.P.;Liau, C.L.;Su, P.H.;Tsao, T.F.;Chang, T.Y.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2009-12-01 |
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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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| 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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| 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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| 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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| 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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| 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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| Universal insertion/deletion-enrich PCR |
Chen, C.K.;Huang, J.K.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-12-01 |
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| Wolf-Hirschhorn (4p-) syndrome: Prenatal diagnosis, molecularcytogenetic characterization and association with a 1.2-Mb microduplicationat 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with anapparently pure 4p deletion |
Chen, C.P.;Su, Y.N.;Chen, Y.Y.;Su, J.W.;Chern, S.R.;Chen, Y.T.;Chen, W.L.;Chen, L.F.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-12-01 |
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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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| Universal insertion/deletion-enrich PCR |
Chen, C.K.;Huang, J.K.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-12-01 |
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| Wolf-Hirschhorn (4p-) syndrome: Prenatal diagnosis, molecularcytogenetic characterization and association with a 1.2-Mb microduplicationat 8p22-p21.3 and a 1.1-Mb microduplication at 10p15.3 in a fetus with anapparently pure 4p deletion |
Chen, C.P.;Su, Y.N.;Chen, Y.Y.;Su, J.W.;Chern, S.R.;Chen, Y.T.;Chen, W.L.;Chen, L.F.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2011-12-01 |
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| Mosaic ring chromosome 21, monosomy 21, and isodicentric ringchromosome 21: Prenatal diagnosis, molecular cytogenetic characterization,and association with 2-Mb deletion of 21q21.1-q21.2 and 5-Mb deletion of21q22.3 |
Chen, C.P.;Lin, Y.H.;Chou, S.Y.;Su, Y.N.;Chern, S.R.;Chen, Y.T.;Town, D.D.;Chen, W.L.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2012-03-01 |
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| Rapid aneuploidy diagnosis of partial trisomy 7q (7q34->qter) andpartial monosomy 10q (10q26.12->qter) by array comparative genomichybridization using uncultured amniocytes |
Chen, C.P.;Lin, S.P.;Su, Y.N.;Tsai, F.J.;Wu, P.C.;Town, D.D.;Chen, L.F.;Lee, M.S.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2012-03-01 |
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| Inv dup del(10q): Identification by fluorescence in situ hybridizationand array comparative genomic hybridization in a fetus with two concurrentchromosomal rearrangements |
Chen, C.P.;Chen, M.;Su, Y.N.;Huang, J.P.;Ma, G.C.;Chang, S.P.;Chern, S.R.;Chen, Y.T.;Su, J.W.;Lee, C.C.;Town, D.D.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2012-06-01 |
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| Pure partial monosomy 3p (3p25.3 -> pter): Prenatal diagnosis and arraycomparative genomic hybridization characterization |
Chen, C.P.;Su, Y.N.;Chen, C.Y.;Su, J.W.;Chern, S.R.;Town, D.D.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2012-09-01 |
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| Prenatal diagnosis of a distal 3p deletion associated withfetoplacental chromosomal discrepancy and confined placental mosaicismdetected by array comparative genomic hybridization |
Chen, C.P.;Chen, Y.Y.;Chern, S.R.;Wu, P.S.;Su, J.W.;Chen, W.L.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2013-06-01 |
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| De novo unbalanced translocation resulting in monosomy for distal 5p(5p14.1 -> pter) and 14q (14q32.31 -> qter) associated with fetal nuchaledema, microcephaly, intrauterine growth restriction, and single umbilicalartery: Prenatal diagnosis and molecular cytogenetic characterization |
Chen, C.P.;Fu, C.H.;Chern, S.R.;Wu, P.S.;Su, J.W.;Lee, C.C.;Lee, M.S.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2013-09-01 |
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| De novo unbalanced translocation resulting in monosomy for distal 5p(5p14.1 -> pter) and 14q (14q32.31 -> qter) associated with fetal nuchaledema, microcephaly, intrauterine growth restriction, and single umbilicalartery: Prenatal diagnosis and molecular cytogenetic characterization |
Chen, C.P.;Fu, C.H.;Chern, S.R.;Wu, P.S.;Su, J.W.;Lee, C.C.;Lee, M.S.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2013-09-01 |
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| Chromosomal deletions detected at amniocentesis |
Lin, C.J.;Chen, C.P.;Chien, S.C.;Lee, C.C.;Town, D.D.;Chen, W.L.;Chen, L.F.;Lee, M.S.;Pan, C.W.;Lin, K.C.;Yeh, T.T.; |
Taiwanese Journal of Obstetrics and Gynecology |
2014-03-01 |
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| A 1.37-Mb 12p11.22-p11.21 deletion coincident with a 367-kb 22q11.2duplication detected by array comparative genomic hybridization in anadolescent girl with autism and difficulty in self-care of menstruation |
Chen, C.P.;Lin, S.P.;Chern, S.R.;Wu, P.S.;Su, J.W.;Lee, C.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2014-03-01 |
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| Prenatal diagnosis of a de novo 9p terminal chromosomal deletion in afetus with major congenital anomalies |
Hou, W.C.;Chen, C.P.;Hwang, K.S.;Chen, Y.C.;Lai, Y.J.;Tien, C.Y.;Su, H.Y.; |
Taiwanese Journal of Obstetrics and Gynecology |
2014-12-01 |
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| Prenatal diagnosis of 17q12 duplication and deletion syndrome in twofetuses with congenital anomalies |
Li, R.;Fu, F.;Zhang, Y.L.;Li, D.Z.;Liao, C.; |
Taiwanese Journal of Obstetrics and Gynecology |
2014-12-01 |
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| Distal 3p duplication and terminal 7q deletion associated with nuchaledema and cyclopia in a fetus and a review of the literature |
Chen, C.P.;Huang, M.C.;Chern, S.R.;Kuo, Y.L.;Chen, Y.N.;Wu, P.S.;Chen, L.F.;Pan, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2015-06-01 |
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| Prenatal diagnosis and array comparative genomic hybridizationcharacterization of interstitial deletions of 8q23.3-q24.11 and 8q24.13associated with Langer-Giedion syndrome, Cornelia de Lange syndrome andhaploinsufficiency of TRPS1, RAD21 and EXT1 |
Chen, C.P.;Lin, M.H.;Chen, Y.Y.;Chern, S.R.;Chen, Y.N.;Wu, P.S.;Pan, C.W.;Lee, M.S.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2015-10-01 |
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| Prenatal diagnosis of hemivertebrae-A likely association with 7qdeletion |
Song, Y.Q.;Chen, M.;Yang, Z.l.;He, W.Y.;Liu, W.Q.;Li, Y.;Gong, Y.F.;Wang, J.Y.;Sun, X.F.;Chen, X.J.; |
Taiwanese Journal of Obstetrics and Gynecology |
2016-02-01 |
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| Prenatal diagnosis of 22q11.2 deletion syndrome associated with rightaortic arch, left ductus arteriosus, cardiomegaly, and pericardial effusion |
Chen, Y.N.;Chen, C.P.;Ko, T.M.;Wang, L.K.;Wu, P.C.;Chang, T.Y.;Wu, P.S.;Yang, C.W.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2016-02-01 |
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| Prenatal diagnosis and molecular cytogenetic characterization of denovo partial monosomy 3p (3p26.3->pter) and partial trisomy 16q(16q23.1->qter) |
Chen, C.P.;Hung, F.Y.;Chern, S.R.;Wu, P.S.;Chen, Y.N.;Chen, S.W.;Lee, C.C.;Wang, W.; |
Taiwanese Journal of Obstetrics and Gynecology |
2016-04-01 |
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