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Journal Abstract Search

460 related items for PubMed ID: 8734817

  • 21. Prenatal diagnosis of Prader-Willi syndrome using PW71 methylation analysis--uniparental disomy and the significance of residual trisomy 15.
    Slater HR, Vaux C, Pertile M, Burgess T, Petrovic V.
    Prenat Diagn; 1997 Feb; 17(2):109-13. PubMed ID: 9061757
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  • 25. Confined placental mosaicism for trisomy 14 and maternal uniparental disomy in association with elevated second trimester maternal serum human chorionic gonadotrophin and third trimester fetal growth restriction.
    Towner DR, Shaffer LG, Yang SP, Walgenbach DD.
    Prenat Diagn; 2001 May; 21(5):395-8. PubMed ID: 11360282
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  • 26. Trisomy 16 and trisomy 16 Mosaicism: a review.
    Benn P.
    Am J Med Genet; 1998 Sep 01; 79(2):121-33. PubMed ID: 9741470
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  • 28. Two cases of confined placental mosaicism for chromosome 4, including one with maternal uniparental disomy.
    Kuchinka BD, Barrett IJ, Moya G, Sánchez JM, Langlois S, Yong SL, Kalousek DK, Robinson WP.
    Prenat Diagn; 2001 Jan 01; 21(1):36-9. PubMed ID: 11180238
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  • 29. Complete discrepancy between QF-PCR analysis of uncultured villi and karyotyping of cultured cells in the prenatal diagnosis of trisomy 21 in three CVS.
    Waters JJ, Mann K, Grimsley L, Ogilvie CM, Donaghue C, Staples L, Hills A, Adams T, Wilson C.
    Prenat Diagn; 2007 Apr 01; 27(4):332-9. PubMed ID: 17286305
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  • 30. Mosaicism for trisomy 12: four cases with varying outcomes.
    Bischoff FZ, Zenger-Hain J, Moses D, Van Dyke DL, Shaffer LG.
    Prenat Diagn; 1995 Nov 01; 15(11):1017-26. PubMed ID: 8606880
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  • 31. Detection of maternal uniparental disomy 9 in association with low-level mosaic trisomy 9 at amniocentesis in a pregnancy associated with intrauterine growth restriction, abnormal first-trimester screening result (low PAPP-A and low PlGF), maternal preeclampsia and a favorable outcome.
    Chen CP, Chern SR, Wu PS, Chen SW, Wu FT, Chen LF, Chen YY, Wang W.
    Taiwan J Obstet Gynecol; 2022 Jan 01; 61(1):141-145. PubMed ID: 35181026
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  • 32. Mosaic trisomy 9 at amniocentesis: prenatal diagnosis and molecular genetic analyses.
    Chen CP, Lin HM, Su YN, Chern SR, Tsai FJ, Wu PC, Lee CC, Chen YT, Lee MS, Pan CW, Wang W.
    Taiwan J Obstet Gynecol; 2010 Sep 01; 49(3):341-50. PubMed ID: 21056321
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  • 34. Molecular-cytogenetic investigations of ten term placentae in cases of prenatally diagnosed mosaicism.
    Schubert R, Raff R, Schwanitz G.
    Prenat Diagn; 1996 Oct 01; 16(10):907-13. PubMed ID: 8938059
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  • 38. Cytogenetic and molecular genetic characterization of trisomy 20 mosaicism in fetal blood and tissues.
    Micale MA, Wolff DJ, Dickerman LH, Redline R, Conroy JM, Schwartz S.
    Prenat Diagn; 1996 Oct 01; 16(10):893-7. PubMed ID: 8938057
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  • 39. Identification of a case of maternal uniparental disomy of chromosome 10 associated with confined placental mosaicism.
    Jones C, Booth C, Rita D, Jazmines L, Spiro R, McCulloch B, McCaskill C, Shaffer LG.
    Prenat Diagn; 1995 Sep 01; 15(9):843-8. PubMed ID: 8559755
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  • 40. A CASE OF CONFINED PLACENTAL MOSAICISM WITH TRISOMY 15 ASSOCIATED WITH TURNER SYNDROME.
    Ekici C, Sahin Y, Yaykasli KO, Melekoglu R, Sahin N, Yuksel S.
    Genet Couns; 2016 Sep 01; 27(4):485-488. PubMed ID: 30226967
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