| 篇名 | 作者 | 刊名 | 出版年 | 查看 |
|---|
| Loss of heterozygosity on chromosome 17q11-21 in cancers of women who haveboth breast and ovarian cancer |
Schildkraut, J.M.;Collins, N.K.;Dent, G.A.;Tucker, J.A.;Barrett, J.C.;Berchuck, A.;Boyd, J.; |
American Journal of Obstetrics and Gynecology |
1995-03-01 |
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| Role of prenatal ultrasonography in women with positive screen for Downsyndrome on the basis of maternal serum markers |
Nyberg, D.A.;Luthy, D.A.;Cheng, E.Y.;Sheley, R.C.;Resta, R.G.;Williams, M.A.; |
American Journal of Obstetrics and Gynecology |
1995-10-01 |
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| Pericentric inversion of chromosome 7 associated with recurrent abortion |
Imai, A.;Tamaya, T.; |
International Journal of Gynecology & Obstetrics |
1996-02-01 |
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| Evaluating sex chromosome content of sorted human sperm samples withuse of dual-color fluorescence in situ hybridization |
Richards, W.;Dobin, S.M.;Malone, V.;Knight, A.B.;Kuehl, T.J.; |
American Journal of Obstetrics and Gynecology |
1997-06-01 |
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| Case Report: Denovo inherited 18p deletion in a mother-fetus pair withextremely variable expression, confirmed by fluorescence in situhybridization (FISH) analysis. |
Tonk, V.;Krishna, J.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
1997-06-01 |
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| Case Report: Denovo inherited 18p deletion in a mother-fetus pair withextremely variable expression, confirmed by fluorescence in situhybridization (FISH) analysis. |
Tonk, V.;Krishna, J.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
1997-06-01 |
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| Case report: Denovo inherited 18p deletion in a mother-fetus pair withextremely variable expression, confirmed by fluorescence in situhybridization (FISH) analysis |
Tonk, V.;Krishna, J.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
1997-06-01 |
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| Fluorescence microsatellite analysis to study the parental origin of thesupernumerary chromosome in Down's syndrome |
Ko, T.M.;Hwa, H.L.;Tseng, L.H.;Lin, Y.W.;Cheung, Y.P.; |
International Journal of Gynecology & Obstetrics |
1998-05-12 |
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| Genetic basis of uterine leiomyoma: involvement of high mobility groupprotein genes |
Van de Ven, W.J.M.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
1998-12-01 |
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| Structural chromosome rearrangements in couples with recurrent fetalwastage |
Fryns, J.-P.;Van Buggenhout, G.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
1998-12-01 |
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| Genetic abnormalities and male infertility. A comprehensive review |
Thielemans, B.F.J.;Spiessens, C.;D'Hooghe, T.;Vanderschueren, D.;Legius, E.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
1998-12-01 |
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| Structural chromosome rearrangements in couples with recurrent fetalwastage |
Fryns, J.P.;Van Buggenhout, G.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
1998-12-01 |
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| Genetic abnormalities and male infertility. A comprehensive review. |
Thielemans, B.F.J.;Spiessens, C.;D'Hooghe, T.;Vanderschueren, D.;Legius, E.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
1998-12-01 |
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| Genetic basis of uterine leiomyoma: involvement of high mobility groupprotein genes |
Van de Ven, W.J.M.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
1998-12-01 |
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| Genetic aspects of miscarriage |
Goddijn, M.;Leschot, N.J.; |
Best Practice & Research in Clinical Obstetrics and Gynaecology |
2000-10-01 |
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| Genetic aspects of miscarriage |
Goddijn, M.;Leschot, N.J.; |
Best Practice & Research in Clinical Obstetrics and Gynaecology |
2000-10-01 |
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| Genetic aspects of miscarriage |
Goddijn, M.;Leschot, N.J.; |
Best Practice & Research in Clinical Obstetrics and Gynaecology |
2000-10-01 |
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| Prenatal diagnosis: molecular genetics and cytogenetics |
Bui, T.-H.;Blennow, E.;Nordenskjold, M.; |
Best Practice & Research in Clinical Obstetrics and Gynaecology |
2002-10-01 |
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| Cytogenetic analysis of uterine leiomyoma: the size, histopathology andGnRHa-response in relation to chromosome karyotype |
Kataoka, S.;Yamada, H.;Hoshi, N.;Kudo, M.;Hareyama, H.;Sakuragi, N.;Fujimoto, S.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
2003-09-10 |
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| Cytogenetic analysis of uterine leiomyoma: the size, histopathology andGnRHa-response in relation to chromosome karyotype |
Kataoka, S.;Yamada, H.;Hoshi, N.;Kudo, M.;Hareyama, H.;Sakuragi, N.;Fujimoto, S.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
2003-09-10 |
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| Human sex differentiation and its abnormalities |
Migeon, C.J.;Wisniewski, A.B.; |
Best Practice & Research in Clinical Obstetrics and Gynaecology |
2003-02-01 |
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| The clinical use of karyotyping spontaneous abortions |
Hogge, W.A.;Byrnes, A.L.;Lanasa, M.C.;Surti, U.; |
American Journal of Obstetrics and Gynecology |
2003-08-01 |
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| Parental decisions following the prenatal diagnosis of sex chromosomeabnormalities |
Hamamy, H.A.;Dahoun, S.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
2004-09-10 |
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| Parental decisions following the prenatal diagnosis of sex chromosomeabnormalities |
Hamamy, H.A.;Dahoun, S.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
2004-09-10 |
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| Genetic aspects of human male infertility: the frequency of chromosomalabnormalities and Y chromosome microdeletions in severe male factorinfertility |
Vicdan, A.;Vicdan, K.;Gunalp, S.;Kence, A.;Akarsu, C.;Isik, A.Z.;Sozen, E.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
2004-11-10 |
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| Genetic aspects of human male infertility: the frequency of chromosomalabnormalities and Y chromosome microdeletions in severe male factorinfertility |
Vicdan, A.;Vicdan, K.;Gunalp, S.;Kence, A.;Akarsu, C.;Isik, A.Z.;Sozen, E.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
2004-11-10 |
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| FISHing for acrocentric associations between chromosomes 14 and 21 in humanoogenesis |
Cheng, E.Y.;Naluai-Cecchini, T.; |
American Journal of Obstetrics and Gynecology |
2004-06-01 |
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| How unexpected are unexpected findings in prenatal cytogenetic diagnosis? Aliterature review |
Zwieten, M.C.B.v.;Willems, D.L.;Litjens, L.L.;Schuring-Blom, H.G.;Leschot, N.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
2005-05-01 |
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| How unexpected are unexpected findings in prenatal cytogeneticdiagnosis? A literature review |
Zwieten, M.C.B.v.;Willems, D.L.;Litjens, L.L.;Schuring-Blom, H.G.;Leschot, N.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
2005-05-01 |
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| Independent clonal origin of multiple uterine leiomyomas that wasdetermined by X chromosome inactivation and microsatellite analysis |
Canevari, R.A.;Pontes, A.;Rosa, F.E.;Rainho, C.A.;Rogatto, S.R.; |
American Journal of Obstetrics and Gynecology |
2005-10-01 |
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| Ring Chromosome 7 Presenting with Intrauterine Growth Restriction andMultiple Anomalies |
Tsai, P.Y.;Lin, Y.H.;Chang, C.H.;Chang, F.M.;Kuo, P.L.; |
Taiwanese Journal of Obstetrics and Gynecology |
2005-09-01 |
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| Cytogenetic analysis of azoospermic patients: karyotype comparison ofperipheral blood lymphocytes and testicular tissue |
Stipoljev, F.;Vujisic, S.;Parazajder, J.;Hafner, D.;Jezek, D.;Sertic, J.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
2006-02-01 |
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| Cytogenetic analysis of azoospermic patients: karyotype comparison ofperipheral blood lymphocytes and testicular tissue |
Stipoljev, F.;Vujisic, S.;Parazajder, J.;Hafner, D.;Jezek, D.;Sertic, J.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
2006-02-01 |
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| Detection of Chromosome Aberrations in the Second Trimester UsingGenetic Amniocentesis: Experience During 1995-2004 |
Tseng, J.J.;Chou, M.M.;Lo, F.C.;Lai, H.Y.;Chen, M.H.;Ho, E.S.C.; |
Taiwanese Journal of Obstetrics and Gynecology |
2006-03-01 |
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| Recurrent spontaneous abortion and skewed X-inactivation: is there anassociation? |
Hogge, W.A.;Prosen, T.L.;Lanasa, M.C.;Huber, H.A.;Reeves, M.F.; |
American Journal of Obstetrics and Gynecology |
2007-04-01 |
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| Recurrent spontaneous abortion and skewed X-inactivation: is there anassociation? |
Hogge, W.A.;Prosen, T.L.;Lanasa, M.C.;Huber, H.A.;Reeves, M.F.; |
American Journal of Obstetrics and Gynecology |
2007-04-01 |
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| Prenatal Diagnosis of mos45,X/46,X,+mar in a Fetus With Normal MaleExternal Genitalia and a Literature Review |
Chien, S.C.;Chen, C.P.;Lin, C.C.;Huang, L.C.;Hsieh, C.T.;Tsai, F.J.; |
Taiwanese Journal of Obstetrics and Gynecology |
2009-09-01 |
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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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| 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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| 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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| 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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| Prenatal Diagnosis and Molecular Cytogenetic Characterization of aSmall Supernumerary Marker Chromosome Derived From Chromosome 8 |
Chen, C.P.;Chen, M.;Ko, T.M.;Ma, G.C.;Tsai, F.J.;Tsai, M.S.;Wu, P.C.;Lee, C.C.;Chen, L.F.;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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| DYZ1 copy number variation, Y chromosome polymorphism and earlyrecurrent spontaneous abortion/early embryo growth arrest |
Yan, J.;Fan, L.;Zhao, Y.;You, L.;Wang, L.;Zhao, H.;Li, Y.;Chen, Z.J.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
2011-12-01 |
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| DYZ1 copy number variation, Y chromosome polymorphism and earlyrecurrent spontaneous abortion/early embryo growth arrest |
Yan, J.;Fan, L.;Zhao, Y.;You, L.;Wang, L.;Zhao, H.;Li, Y.;Chen, Z.J.; |
European Journal of Obstetrics & Gynecology and Reproductive Biology |
2011-12-01 |
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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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| 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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| 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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