BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

337 related articles for article (PubMed ID: 11783350)

  • 21. False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite probe (D18Z1) to chromosome 2.
    Collin A; Sladkevicius P; Soller M
    Prenat Diagn; 2009 Dec; 29(13):1279-81. PubMed ID: 19911414
    [No Abstract]   [Full Text] [Related]  

  • 22. Rapid prenatal diagnosis of Down syndrome using quantitative fluorescence in situ hybridization on interphase nuclei.
    Truong K; Gibaud A; Dupont JM; Guilly MN; Soussaline F; Dutrillaux B; Malfoy B
    Prenat Diagn; 2003 Feb; 23(2):146-51. PubMed ID: 12575023
    [TBL] [Abstract][Full Text] [Related]  

  • 23. [Interphase FISH test as a rapid test for trisomies in amniotic fluid--results of a prospective study].
    Bink K; Pauer HU; Bartels I
    Z Geburtshilfe Neonatol; 2000; 204(1):8-13. PubMed ID: 10721180
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Re: Cross-hybridization of the chromosome 13/21 alpha satellite DNA probe to chromosome 22 in the prenatal screening of common aneuploidies by FISH.
    Blancato JK
    Prenat Diagn; 1996 Aug; 16(8):769-70. PubMed ID: 8878290
    [No Abstract]   [Full Text] [Related]  

  • 25. [Application of multicolor primed in situ labeling in simultaneous identification of chromosomes 18, X and Y in uncultured amniocytes].
    Deng L; Ding XP; Nie Y; Hu Y; Ren HJ
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Aug; 26(4):439-42. PubMed ID: 20017312
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Molecular cytogenetic detection of trisomy 21 in interphase nuclei and metaphase chromosomes.
    Li F; Fang W; Wu B; Wang J; Zhong H; Heng W
    Chin Med J (Engl); 1999 Sep; 112(9):840-4. PubMed ID: 11717958
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Prenatal exclusion of segmental trisomy in familial chromosome 21 pericentric inversion by fluorescence in situ hybridization.
    Tardy EP; Tóth A; Kosztolányi G
    Prenat Diagn; 1997 Sep; 17(9):871-3. PubMed ID: 9316133
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screening.
    Graf MD; Gill P; Krew M; Schwartz S
    Prenat Diagn; 2002 Aug; 22(8):645-8. PubMed ID: 12210569
    [TBL] [Abstract][Full Text] [Related]  

  • 29. Rapid prenatal diagnosis of chromosome aneuploidies by interphase fluorescence in situ hybridization: a one-year clinical experience with high-risk and urgent fetal and postnatal samples.
    Bryndorf T; Lundsteen C; Lamb A; Christensen B; Philip J
    Acta Obstet Gynecol Scand; 2000 Jan; 79(1):8-14. PubMed ID: 10646809
    [TBL] [Abstract][Full Text] [Related]  

  • 30. [Application of fluorescence in situ hybridization in the diagnosis of genetic diseases].
    Zhao L; Li H; Xue YQ; Pan JL; Wu YF; Lu M
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):611-4. PubMed ID: 15583994
    [TBL] [Abstract][Full Text] [Related]  

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

  • 32. Prenatal diagnosis of trisomy 21 using interphase fluorescence in situ hybridization of post-replicated cells with site-specific cosmid and cosmid contig probes.
    Soloviev IV; Yurov YB; Vorsanova SG; Fayet F; Roizes G; Malet P
    Prenat Diagn; 1995 Mar; 15(3):237-48. PubMed ID: 7784382
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Application of fluorescence insitu hybridization technique for prenatal diagnosis of chromosome abnormality in amniotic cells].
    Huang Y; Sun X; Li Q
    Zhonghua Fu Chan Ke Za Zhi; 1999 Mar; 34(3):153-5. PubMed ID: 11263185
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Prenatal detection of trisomy 21 in uncultured amniocytes by fluorescence in situ hybridization: a prospective study.
    Spathas DH; Divane A; Maniatis GM; Ferguson-Smith ME; Ferguson-Smith MA
    Prenat Diagn; 1994 Nov; 14(11):1049-54. PubMed ID: 7877952
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Simultaneous identification of chromosomes 18, X and Y in uncultured amniocytes by using multi-primed in situ labelling technique.
    Gadji M; Krabchi K; Drouin R
    Clin Genet; 2005 Jul; 68(1):15-22. PubMed ID: 15952981
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Rapid prenatal diagnostics in the interphase nucleus: procedure and cut-off rates.
    Liehr T; Ziegler M
    J Histochem Cytochem; 2005 Mar; 53(3):289-91. PubMed ID: 15750004
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Prenatal diagnosis of chromosomal aneuploidies by fluorescence in situ hybridization on uncultured amniotic cells: experience with 630 samples.
    Mercier S; Bresson JL
    Ann Genet; 1995; 38(3):151-7. PubMed ID: 8540686
    [TBL] [Abstract][Full Text] [Related]  

  • 38. The clinical application of interphase FISH in prenatal diagnosis.
    Pergament E; Chen PX; Thangavelu M; Fiddler M
    Prenat Diagn; 2000 Mar; 20(3):215-20. PubMed ID: 10719324
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Rapid prenatal diagnosis of trisomy 18 and triploidy in interphase nuclei of uncultured amniocytes by non-radioactive in situ hybridization.
    Christensen B; Bryndorf T; Philip J; Lundsteen C; Hansen W
    Prenat Diagn; 1992 Apr; 12(4):241-50. PubMed ID: 1614982
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Defining the efficiency of fluorescence in situ hybridization on uncultured amniocytes on a retrospective cohort of 27407 prenatal diagnoses.
    Lewin P; Kleinfinger P; Bazin A; Mossafa H; Szpiro-Tapia S
    Prenat Diagn; 2000 Jan; 20(1):1-6. PubMed ID: 10701842
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 17.