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總筆數:22

篇名作者刊名出版年查看
Septate uterus with cervical duplication and longitudinal vaginal septum: areport of three new cases Balasch, J.;Moreno, E.;Martinez-Roman, S.;Molini, J.L.;Torne, A.;Sanchez-Martin, F.;Vanrell, J.A.; European Journal of Obstetrics & Gynecology and Reproductive Biology 1996-04-01 查看
Septate uterus with cervical duplication and longitudinal vaginalseptum: a report of three new cases Balasch, J.;Moreno, E.;Martinez-Roman, S.;Molini, J.L.;Torne, A.;Sanchez-Martin, F.;Vanrell, J.A.; European Journal of Obstetrics & Gynecology and Reproductive Biology 1996-04-01 查看
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 查看
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 查看
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 查看
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 查看
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 查看
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 查看
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 查看
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 查看
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 查看
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 查看
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 查看
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 查看
Prenatal diagnosis and molecular cytogenetic characterization ofmosaicism for a small supernumerary marker chromosome derived from ringchromosome 2 Chen, C.P.;Chen, M.;Chern, S.R.;Wu, P.S.;Chang, S.P.;Lee, D.J.;Chen, Y.T.;Chen, L.F.;Su, J.W.;Hwa-Ruey Hsieh, A.;Hwa-Jiun Hsieh, A.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2012-09-01 查看
Prenatal diagnosis and molecular cytogenetic characterization of a denovo interstitial duplication of 11q (11q22.3->q23.3) associated withabnormal maternal serum biochemistry Chen, C.P.;Su, Y.N.;Lin, S.P.;Chern, S.R.;Su, J.W.;Chen, Y.T.;Lee, M.S.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2013-03-01 查看
Prenatal diagnosis and molecular cytogenetic characterization of a denovo interstitial duplication of 14q (14q31.3->q32.12) associated withabnormal maternal serum biochemistry Chen, C.P.;Hwang, K.S.;Su, H.Y.;Lin, S.P.;Su, Y.N.;Chern, S.R.;Su, J.W.;Chen, Y.T.;Chen, W.L.;Wang, W.; Taiwanese Journal of Obstetrics and Gynecology 2013-03-01 查看
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 查看
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 查看
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 查看
Two girls with a de novo Xq rearrangement of paternal origin:t(X;9)(q24;q12) or rea(X)dup q Vasquez-Velasquez, A.I.;Rivera, H.;Castro, A.G.;Jaloma-Cruz, A.R.;Juarez, C.I.;Lara-Navarro, I.J.;Cordova-Fletes, C.;Mendoza- Perez, P.;Garcia-Ortiz, J.E.; Taiwanese Journal of Obstetrics and Gynecology 2016-04-01 查看
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 查看
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