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Journal Abstract Search

248 related items for PubMed ID: 21056320

  • 21. Prenatal diagnosis of mosaic trisomy 8 by amniocentesis in a fetus with ventriculomegaly and dysgenesis of the corpus callosum.
    Chen CP, Hsu CY, Chern SR, Wu PS, Chen SW, Wang W.
    Taiwan J Obstet Gynecol; 2020 Jan; 59(1):127-129. PubMed ID: 32039780
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  • 22. Prenatal diagnosis of mosaicism for trisomy 7 in a single colony at amniocentesis in a pregnancy with a favorable outcome.
    Chen CP, Hung FY, Chern SR, Chen SW, Wu FT, Town DD, Wang W.
    Taiwan J Obstet Gynecol; 2019 Nov; 58(6):852-854. PubMed ID: 31759541
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  • 23. Fetal trisomy 8 mosaicism associated with truncus arteriosus Type I.
    Sherer DM, Dalloul M, Pinard V, Sheu J, Abulafia O.
    Ultrasound Obstet Gynecol; 2017 Oct; 50(4):541-542. PubMed ID: 28093816
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  • 24. 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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  • 27. Prenatal diagnosis of low-level mosaic trisomy 7 by amniocentesis.
    Chen CP, Chern SR, Chen LF, Chen WL, Wang W.
    Prenat Diagn; 2005 Nov 01; 25(11):1067-9. PubMed ID: 16302164
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  • 29. Mosaic trisomy 17 in amniocytes: phenotypic outcome, tissue distribution, and uniparental disomy studies.
    Genuardi M, Tozzi C, Pomponi MG, Stagni ML, Della Monica M, Scarano G, Calvieri F, Torrisi L, Neri G.
    Eur J Hum Genet; 1999 Nov 01; 7(4):421-6. PubMed ID: 10352932
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  • 30. [Detection of mosaic trisomy 9 missed by conventional cytogenetics using SNP-array and fluorescence in situ hybridization].
    Luo Y, Chen S, Li H, Pan L, Shen M, Jin F, Xu C.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2014 Aug 01; 31(4):469-71. PubMed ID: 25119912
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  • 31. A prenatal diagnosis of mosaic trisomy 5 reveals a postnatal complete uniparental disomy of chromosome 5 with multiple congenital anomalies.
    Reittinger AM, Helm BM, Boles DJ, Gadi IK, Schrier Vergano SA.
    Am J Med Genet A; 2017 Sep 01; 173(9):2528-2533. PubMed ID: 28653809
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  • 35. Origin of amnion and implications for evaluation of the fetal genotype in cases of mosaicism.
    Robinson WP, McFadden DE, Barrett IJ, Kuchinka B, Peñaherrera MS, Bruyère H, Best RG, Pedreira DA, Langlois S, Kalousek DK.
    Prenat Diagn; 2002 Dec 01; 22(12):1076-85. PubMed ID: 12454962
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  • 36. Postnatal follow-up of prenatally diagnosed trisomy 16 mosaicism.
    Langlois S, Yong PJ, Yong SL, Barrett I, Kalousek DK, Miny P, Exeler R, Morris K, Robinson WP.
    Prenat Diagn; 2006 Jun 01; 26(6):548-58. PubMed ID: 16683298
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  • 37. Detection of fetal trisomy 9 mosaicism by noninvasive prenatal testing through maternal plasma DNA sequencing.
    Lee CY, Su HJ, Cheng YT, Ku YL, Ngo YG, Chen CM, Ou YC, Lee MC, Shaw SWS.
    Taiwan J Obstet Gynecol; 2018 Aug 01; 57(4):594-597. PubMed ID: 30122585
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  • 40. Prenatal diagnosis and postnatal follow-up of a child with mosaic trisomy 22 with several levels of mosaicism in different tissues.
    Mazza V, Latella S, Fenu V, Ferrari P, Bonilauri C, Santucci S, Percesepe A.
    J Obstet Gynaecol Res; 2010 Oct 01; 36(5):1116-20. PubMed ID: 20722987
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