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Journal Abstract Search

298 related items for PubMed ID: 14974120

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  • 3. Prenatal diagnosis of mos45,X/46,X,+mar in a fetus with normal male external genitalia and a literature review.
    Chien SC, Chen CP, Lin CC, Huang LC, Hsieh CT, Tsai FJ.
    Taiwan J Obstet Gynecol; 2009 Sep; 48(3):292-5. PubMed ID: 19797023
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  • 4. Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis.
    Velissariou V, Antoniadi T, Patsalis P, Christopoulou S, Hatzipouliou A, Donoghue J, Bakou K, Kaminopetros P, Athanassiou V, Petersen MB.
    Prenat Diagn; 2001 Jun; 21(6):484-7. PubMed ID: 11438955
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  • 5. Isodicentric Yp: prenatal diagnosis and outcome in 12 cases.
    Bruyère H, Speevak MD, Winsor EJ, de Fréminville B, Farrell SA, McGowan-Jordan J, McGillivray B, Chitayat D, McFadden D, Adouard V, Terespolsky D, Prieur F, Pantzar T, Hrynchak M.
    Prenat Diagn; 2006 Apr; 26(4):324-9. PubMed ID: 16521154
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  • 6. [Prenatal diagnosis of two pregnancies with risk of chromosomal disorders].
    Cui YX, Huang B, Shi YC, Lu HY, Xia XY, Pan LJ, Huang YF.
    Zhonghua Nan Ke Xue; 2007 Jul; 13(7):624-7. PubMed ID: 17725307
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  • 7. Clinical and molecular cytogenetic studies in three infertile patients with mosaic rearranged Y chromosomes.
    Bettio D, Venci A, Rizzi N, Negri L, Setti PL.
    Hum Reprod; 2006 Apr; 21(4):972-5. PubMed ID: 16484313
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  • 9. Clinical, cytogenetic, and molecular findings in 45,X/47,XX,+18 mosaicism: clinical report and review of the literature.
    Schubert R, Eggermann T, Hofstaetter C, von Netzer B, Knöpfle G, Schwanitz G.
    Am J Med Genet; 2002 Jul 01; 110(3):278-82. PubMed ID: 12116238
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  • 10. Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis.
    Chen CP, Chang SD, Su YN, Chen M, Chern SR, Su JW, Chen YT, Chen WL, Pan CW, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2012 Sep 01; 51(3):405-10. PubMed ID: 23040926
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  • 11. [Genetic analysis of a fetus with with 45,X/46,X,idic(Y)(q11.2) mosaicism].
    Pan F, Zhang W, Zhang W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2024 Aug 10; 41(8):897-902. PubMed ID: 39097269
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  • 13. Molecular cytogenetic analysis of a ring-Y infertile male patient.
    Carvalho FM, Wolfgramm EV, Degasperi I, Verbeno BM, Vianna BA, Chagas FF, Perroni AM, Paula F, Louro ID.
    Genet Mol Res; 2007 Mar 09; 6(1):59-66. PubMed ID: 17469055
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  • 14. Molecular breakpoint analysis and relevance of variable mosaicism in a woman with short stature, primary amenorrhea, unilateral gonadoblastoma, and a 46,X,del(Y)(q11)/45,X karyotype.
    Kotzot D, Dufke A, Tzschach A, Baeckert-Sifeddine IT, Geppert M, Holland H, Florus JM, Froster UG.
    Am J Med Genet; 2002 Sep 15; 112(1):51-5. PubMed ID: 12239720
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  • 15. Isodicentric Y (p11.32) chromosome in an infant with mixed gonadal dysgenesis.
    Aktas D, Alikasifoglu M, Gonc N, Senocak ME, Tuncbilek E.
    Eur J Med Genet; 2006 Sep 15; 49(2):141-9. PubMed ID: 16530711
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  • 16. Noninvasive genotyping of 9 Y-chromosome specific STR loci using circulatory fetal DNA in maternal plasma by multiplex PCR.
    Deng Z, Wu G, Li Q, Zhang X, Liang Y, Li D, Gao S, Lan Y.
    Prenat Diagn; 2006 Apr 15; 26(4):362-8. PubMed ID: 16566058
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  • 17. [Screening for Y chromosome sequences in patients with Turner syndrome].
    Ferrão L, Lopes ML, Limbert C, Marques B, Boieiro F, Silva M, Marques R, Lavinha J, Mota A, Gonçalves J.
    Acta Med Port; 2002 Apr 15; 15(2):89-100. PubMed ID: 15524154
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  • 18. Molecular and cytogenetic characterization of a structural rearrangement of the Y chromosome in an azoospermic man.
    Valetto A, Bertini V, Rapalini E, Baldinotti F, Di Martino D, Simi P.
    Fertil Steril; 2004 May 15; 81(5):1388-90. PubMed ID: 15136108
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  • 19. Inv dup del(9p): prenatal diagnosis and molecular cytogenetic characterization by fluorescence in situ hybridization and array comparative genomic hybridization.
    Chen CP, Su YN, Chern SR, Hsu CY, Tsai FJ, Wu PC, Lee CC, Chen YT, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2011 Mar 15; 50(1):67-73. PubMed ID: 21482378
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  • 20. A case of 48,XXYY syndrome detected prenatally by QF-PCR.
    Zhang QS, Li DZ.
    J Matern Fetal Neonatal Med; 2009 Dec 15; 22(12):1214-6. PubMed ID: 19916722
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