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Journal Abstract Search

110 related items for PubMed ID: 20029221

  • 21. Minimally-invasive early prenatal diagnosis using fluorescence in situ hybridization on samples from uterine lavage.
    Chang SD, Lin SL, Chu KK, Hsi BL.
    Prenat Diagn; 1997 Nov; 17(11):1019-25. PubMed ID: 9399349
    [Abstract] [Full Text] [Related]

  • 22. Prenatal diagnosis of isochromosome 21p and isochromosome 21q in a fetus with Down syndrome.
    Yakut S, Sanhal C, Manguoglu E, Cetin Z.
    Genet Couns; 2014 Nov; 25(3):257-64. PubMed ID: 25365847
    [Abstract] [Full Text] [Related]

  • 23. Prenatal diagnosis of partial trisomy 1q using fluorescent in situ hybridization.
    DuPont BR, Huff RW, Ridgway LE, Stratton RF, Moore CM.
    Am J Med Genet; 1994 Mar 01; 50(1):21-7. PubMed ID: 8160748
    [Abstract] [Full Text] [Related]

  • 24. [Rapid prenatal diagnosis of chromosome aneuploidies in 60 uncultured amniotic fluid samples by fluorescence in situ hybridization].
    Wang H, Li H, Wang H, Wang H, Xia Y, Wen J, Long Z, Dai H, Liang D, Xia J, Wu L.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct 01; 25(5):538-41. PubMed ID: 18841567
    [Abstract] [Full Text] [Related]

  • 25. Prenatal findings and molecular cytogenetic analyses of partial trisomy 12q (12q24.32-->qter) and partial monosomy 21q (21q22.2-->qter).
    Chen CP, Chern SR, Lin CC, Wang TH, Li YC, Hsieh LJ, Lee CC, Hua HM, Wang W.
    Prenat Diagn; 2006 Apr 01; 26(4):313-20. PubMed ID: 16506269
    [Abstract] [Full Text] [Related]

  • 26. Fluorescence in situ hybridization of chorionic interphase cells for prenatal screening of Down syndrome.
    Tóth A, Tardy EP, Hajdu K, Bátorfi J, Doszpod J, Egyed J, Gáti I.
    Eur J Obstet Gynecol Reprod Biol; 2001 Jan 01; 94(1):46-50. PubMed ID: 11134825
    [Abstract] [Full Text] [Related]

  • 27. Early and rapid prenatal diagnosis of monosomy 2q36.1 in trophoblast cells.
    Tachdjian G, Aboura A, Brisset S, Dommergues M, Gajdos V, Labrune P.
    Fetal Diagn Ther; 2006 Jan 01; 21(5):428-32. PubMed ID: 16912492
    [Abstract] [Full Text] [Related]

  • 28. [Cytogenetic analysis and phenotype location analysis on the karyotype of a ring chromosome 21 syndrome].
    Zhu XY, Zhao R, Ye ZC, Peng YG, Tan YQ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Dec 01; 22(6):682-3. PubMed ID: 16331572
    [Abstract] [Full Text] [Related]

  • 29. (Potential) false-negative diagnoses in chorionic villi and a review of the literature.
    van den Berg C, Van Opstal D, Polak-Knook J, Galjaard RJ.
    Prenat Diagn; 2006 May 01; 26(5):401-8. PubMed ID: 16538702
    [Abstract] [Full Text] [Related]

  • 30. [Fluorescence in situ hybridization in prenatal diagnosis. First experiences].
    Tardy E, Tóth A, Hajdu K, Gombos S, László J.
    Orv Hetil; 1996 Mar 10; 137(10):523-6. PubMed ID: 8713667
    [Abstract] [Full Text] [Related]

  • 31. [Application of inter-fluorescence in situ hybridization of chromosome 13/21 alpha satellite probe in amniotic cells for prenatal diagnosis trisomy 21 syndrome].
    Li W, Wu Y, Ye Z.
    Zhonghua Fu Chan Ke Za Zhi; 2001 Feb 10; 36(2):76-8. PubMed ID: 11783350
    [Abstract] [Full Text] [Related]

  • 32. Partial trisomy/monosomy 6q in fetal cells and CVS long-term culture not present in CVS short-term culture.
    Wegner RD, Schröck E, Obladen M, Becker R, Stumm M, Sperling K.
    Prenat Diagn; 1996 Aug 10; 16(8):741-8. PubMed ID: 8878285
    [Abstract] [Full Text] [Related]

  • 33. Prenatal diagnosis and molecular cytogenetic analysis of partial monosomy 10q (10q25.3-->qter) and partial trisomy 18q (18q23-->qter) in a fetus associated with cystic hygroma and ambiguous genitalia.
    Chen CP, Chern SR, Wang TH, Hsueh DW, Lee CC, Town DD, Wang W, Ko TM.
    Prenat Diagn; 2005 Jun 10; 25(6):492-6. PubMed ID: 15966044
    [Abstract] [Full Text] [Related]

  • 34. Analysis of a de novo complex chromosome rearrangement involving chromosomes 4, 11, 12 and 13 and eight breakpoints by conventional cytogenetic, fluorescence in situ hybridization and spectral karyotyping.
    Peschka B, Leygraaf J, Hansmann D, Hansmann M, Schröck E, Ried T, Engels H, Schwanitz G, Schubert R.
    Prenat Diagn; 1999 Dec 10; 19(12):1143-9. PubMed ID: 10590433
    [Abstract] [Full Text] [Related]

  • 35. [Analysis of complex chromosomal aberrations in patients with myelodysplastic syndromes using multiplex fluorescence in situ hybridization combined with whole chromosome painting].
    Chen LJ, Li JY, Xiao B, Zhu Y, Liu Q, Pan JL, Qiu HR, Fan L, Zhang SJ, Lu RN, Xu W, Xue YQ.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2007 Dec 10; 24(6):635-9. PubMed ID: 18067073
    [Abstract] [Full Text] [Related]

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  • 37. Fluorescence in situ hybridization: a rapid analysis to verify chromosome aberrations.
    Tocharoentanaphol C, Parinayok R, Punthuwattana N, Kangwanpong D.
    J Med Assoc Thai; 2000 Mar 10; 83 Suppl 1():S76-81. PubMed ID: 10865411
    [Abstract] [Full Text] [Related]

  • 38. Quantification of fetal nucleated cells in maternal blood of pregnant women with a male trisomy 21 fetus using molecular cytogenetic techniques.
    Krabchi K, Gadji M, Samassekou O, Grégoire MC, Forest JC, Drouin R.
    Prenat Diagn; 2006 Jan 10; 26(1):28-34. PubMed ID: 16374897
    [Abstract] [Full Text] [Related]

  • 39. An approach for quantitative assessment of fluorescence in situ hybridization (FISH) signals for applied human molecular cytogenetics.
    Iourov IY, Soloviev IV, Vorsanova SG, Monakhov VV, Yurov YB.
    J Histochem Cytochem; 2005 Mar 10; 53(3):401-8. PubMed ID: 15750029
    [Abstract] [Full Text] [Related]

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