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Journal Abstract Search

193 related items for PubMed ID: 26663059

  • 1. [Misdiagnosis of mosaic tetrasomy 9p in a fetus by single nucleotide polymorphism-based array].
    Wu J, Xie Y, Chen B.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Dec; 32(6):830-3. PubMed ID: 26663059
    [Abstract] [Full Text] [Related]

  • 2. Mosaic tetrasomy 9p at amniocentesis in a pregnancy associated with a favorable fetal outcome, perinatal progressive decrease of the aneuploid cell line and cytogenetic discrepancy in various tissues.
    Chen CP, Chen SW, Chern SR, Wu PS, Wu FT, Pan YT, Lee CC, Pan CW, Chen YY, Wang W.
    Taiwan J Obstet Gynecol; 2023 Jan; 62(1):148-154. PubMed ID: 36720529
    [Abstract] [Full Text] [Related]

  • 3. Mosaic tetrasomy 9p at amniocentesis: prenatal diagnosis, molecular cytogenetic characterization, and literature review.
    Chen CP, Wang LK, Chern SR, Wu PS, Chen YT, Kuo YL, Chen WL, Lee MS, Wang W.
    Taiwan J Obstet Gynecol; 2014 Mar; 53(1):79-85. PubMed ID: 24767652
    [Abstract] [Full Text] [Related]

  • 4. Clinical and molecular delineation of Tetrasomy 9p syndrome: report of 12 new cases and literature review.
    El Khattabi L, Jaillard S, Andrieux J, Pasquier L, Perrin L, Capri Y, Benmansour A, Toutain A, Marcorelles P, Vincent-Delorme C, Journel H, Henry C, De Barace C, Devisme L, Dubourg C, Demurger F, Lucas J, Belaud-Rotureau MA, Amiel J, Malan V, De Blois MC, De Pontual L, Lebbar A, Le Dû N, Germain DP, Pinard JM, Pipiras E, Tabet AC, Aboura A, Verloes A.
    Am J Med Genet A; 2015 Jun; 167(6):1252-61. PubMed ID: 25847481
    [Abstract] [Full Text] [Related]

  • 5. [Improved identification for 5p deletion syndrome and partial trisomy 11q presented in a fetus by SNP array].
    Shi S, Pan G, Yang Y, Yan R, Li W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):195-9. PubMed ID: 27060314
    [Abstract] [Full Text] [Related]

  • 6. First Case Report of Maternal Mosaic Tetrasomy 9p Incidentally Detected on Non-Invasive Prenatal Testing.
    Shu W, Cheng SSW, Xue S, Chan LW, Soong SI, Kan ASY, Cheung SWH, Choy KW.
    Genes (Basel); 2021 Mar 05; 12(3):. PubMed ID: 33807602
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  • 9. [Prenatal diagnosis of women with an adverse reproductive history using both traditional karyotyping and SNP-array].
    Yu HS, Guo H, Shen SS, Li XC, Zhang LP, Fan XF.
    Zhonghua Fu Chan Ke Za Zhi; 2018 Mar 25; 53(3):155-159. PubMed ID: 29609228
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  • 10. Tetrasomy 9p mosaicism associated with a normal phenotype in two cases.
    Papoulidis I, Kontodiou M, Tzimina M, Saitis I, Hamid AB, Klein E, Kosyakova N, Kordass U, Kunz J, Siomou E, Nicolaides P, Orru S, Thomaidis L, Liehr T, Petersen MB, Manolakos E.
    Cytogenet Genome Res; 2012 Mar 25; 136(4):237-41. PubMed ID: 22487875
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  • 11. De novo monosomy 9p24.3-pter and trisomy 17q24.3-qter characterised by microarray comparative genomic hybridisation in a fetus with an increased nuchal translucency.
    Brisset S, Kasakyan S, L'Herminé AC, Mairovitz V, Gautier E, Aubry MC, Benkhalifa M, Tachdjian G.
    Prenat Diagn; 2006 Mar 25; 26(3):206-13. PubMed ID: 16450348
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  • 13. [Genetic study of a fetus with 9p direct duplication deletion syndrome].
    Shi S, Lin S, Lou X, Li W.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Jun 10; 34(3):419-422. PubMed ID: 28604969
    [Abstract] [Full Text] [Related]

  • 14. [Confirmation of a maternal cryptal balanced translocation through analysis of a fetus using microarray].
    Wu J, Xie Y, Lin S, Chen B, Chen J, Zhang Z, Ji Y.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2015 Feb 10; 32(1):69-72. PubMed ID: 25636103
    [Abstract] [Full Text] [Related]

  • 15. [Application of single nucleotide polymorphism-based array analysis for prenatal diagnosis of a fetus with de novo derivative chromosome].
    Wu J, He Z, Zhang Z, Chen B, Xie Y, Lin S.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Oct 10; 33(5):678-81. PubMed ID: 27577222
    [Abstract] [Full Text] [Related]

  • 16. Mosaic Tetrasomy of 9p24.3q21.11 postnatally identified in an infant born with multiple congenital malformations: a case report.
    Pinto IP, Minasi LB, Steckelberg R, da Silva CC, da Cruz AD.
    BMC Pediatr; 2018 Sep 07; 18(1):298. PubMed ID: 30193577
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  • 17. Prenatal diagnosis and molecular cytogenetic characterization of mosaicism for a small supernumerary marker chromosome derived from ring chromosome 2.
    Chen CP, Chen M, Chern SR, Wu PS, Chang SP, Lee DJ, Chen YT, Chen LF, Su JW, Hwa-Ruey Hsieh A, Hwa-Jiun Hsieh A, Wang W.
    Taiwan J Obstet Gynecol; 2012 Sep 07; 51(3):411-7. PubMed ID: 23040927
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  • 18. Diagnosis and clinical delineation of mosaic tetrasomy 5p.
    Blakey-Cheung S, Parker P, Schlaff W, Monseur B, Keppler-Noreuil K, Al-Kouatly HB.
    Eur J Med Genet; 2020 Jan 07; 63(1):103634. PubMed ID: 30797979
    [Abstract] [Full Text] [Related]

  • 19. Brief clinical report: non-mosaic partial tetrasomy and partial trisomy 9.
    Shapiro SD, Hansen KL, Littlefield CA.
    Am J Med Genet; 1985 Feb 07; 20(2):271-6. PubMed ID: 3976720
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  • 20. [Intrauterine growth retardation associated with a mosaic trisomy 20 limited to the placenta. A case report].
    Lacoste-Jugnet N, Depret-Mosser S, Vinatier D, Savary D, Dufour P, Lefebvre-Maunoury C, Monnier JC.
    J Gynecol Obstet Biol Reprod (Paris); 1995 Feb 07; 24(6):606-9. PubMed ID: 8830080
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