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Journal Abstract Search

173 related items for PubMed ID: 29047159

  • 41. [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; 31(4):469-71. PubMed ID: 25119912
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  • 44. Mosaic trisomy 22 in a 4-year-old boy with congenital heart disease and general hypotrophy: A case report.
    Kalayinia S, Shahani T, Biglari A, Maleki M, Rokni-Zadeh H, Razavi Z, Mahdieh N.
    J Clin Lab Anal; 2019 Feb; 33(2):e22663. PubMed ID: 30259573
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  • 48. Supernumerary marker chromosomes (SMC) and uniparental disomy (UPD): coincidence or consequence?
    Kotzot D.
    J Med Genet; 2002 Oct; 39(10):775-8. PubMed ID: 12362039
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  • 49. Monozygotic twins discordant for trisomy 21: Discussion of etiological events involved.
    Chang YL, Yi WP, Chao AS, Chen KJ, Cheng PJ, Wang TH, Chang SD.
    Taiwan J Obstet Gynecol; 2017 Oct; 56(5):681-685. PubMed ID: 29037558
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  • 51. A child with complementary mosaic trisomy 8 and mosaic trisomy 21; clinical description of Warkany-Down syndrome and mechanism of origin.
    McGregor-Schuerman M, Lo Fo Sang A, Bihari S, Ramdajal N, Suijkerbuijk RF, van Ravenswaaij-Arts CM.
    Eur J Med Genet; 2020 Jun; 63(6):103922. PubMed ID: 32240827
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  • 52. Transfusion medicine illustrated: Mosaic Trisomy 9 in an infant with mixed-field ABO blood grouping.
    Lockhart EL, Combs MR, Buck A, Horn S, Deak K.
    Transfusion; 2013 Sep; 53(9):1884. PubMed ID: 24015938
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  • 53. Trisomy 9 mosaic syndrome: Sixteen additional patients with new and/or less commonly reported features, literature review, and suggested clinical guidelines.
    Li M, Glass J, Du X, Dubbs H, Harr MH, Falk M, Smolarek T, Hopkin RJ, Zackai E, Sheppard SE.
    Am J Med Genet A; 2021 Aug; 185(8):2374-2383. PubMed ID: 33969943
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  • 54. Prenatal diagnosis of low-level trisomy 15 mosaicism with a favorable outcome.
    Zhao Q, Dong H, Huang L, Liang X, Zhang Z.
    Taiwan J Obstet Gynecol; 2020 Jul; 59(4):615-616. PubMed ID: 32653142
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  • 55. Postnatal Identification of Trisomy 21: An Overview of 7,133 Postnatal Trisomy 21 Cases Identified in a Diagnostic Reference Laboratory in China.
    Zhao W, Chen F, Wu M, Jiang S, Wu B, Luo H, Wen J, Hu C, Yu S.
    PLoS One; 2015 Jul; 10(7):e0133151. PubMed ID: 26176847
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  • 57. Mosaic trisomy 8 syndrome with a novel finding of ectopic kidney.
    Aykut A, Cogulu O, Ozkinay F.
    Genet Couns; 2012 Jul; 23(1):77-80. PubMed ID: 22611646
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  • 58. Uniparental disomy and the phenotype of mosaic trisomy 20: a new case and review of the literature.
    Powis Z, Erickson RP.
    J Appl Genet; 2009 Jul; 50(3):293-6. PubMed ID: 19638687
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