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376 related items for PubMed ID: 10719324
1. 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 [Abstract] [Full Text] [Related]
2. 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 [Abstract] [Full Text] [Related]
3. [Diagnosis of aneuploidy with fluorescence in situ hybridization (FISH); value in pregnancies with increased risk for chromosome aberrations]. Ulmer R, Pfeiffer RA, Kollert A, Beinder E. Z Geburtshilfe Neonatol; 2000 Jan; 204(1):1-7. PubMed ID: 10721179 [Abstract] [Full Text] [Related]
4. [Prenatal chromosome analysis using the FISH technique allows fetal aneuploidy detection within a few hours]. Steinborn A, Röddiger S, Born HJ, Baier P, Halberstadt E. Z Geburtshilfe Neonatol; 1996 Jan; 200(5):186-90. PubMed ID: 9035828 [Abstract] [Full Text] [Related]
5. Residual risk for cytogenetic abnormalities after prenatal diagnosis by interphase fluorescence in situ hybridization (FISH). Homer J, Bhatt S, Huang B, Thangavelu M. Prenat Diagn; 2003 Jul; 23(7):566-71. PubMed ID: 12868085 [Abstract] [Full Text] [Related]
6. First-trimester prenatal diagnosis performed on pregnant women with fetal ultrasound abnormalities: the reliability of interphase fluorescence in situ hybridization (FISH) on mesenchymal core for the main aneuploidies. Toutain J, Epiney M, Begorre M, Dessuant H, Vandenbossche F, Horovitz J, Saura R. Eur J Obstet Gynecol Reprod Biol; 2010 Apr; 149(2):143-6. PubMed ID: 20045588 [Abstract] [Full Text] [Related]
7. Fluorescence in situ hybridization (FISH) for rapid detection of aneuploidy: experience in 911 prenatal cases. Weremowicz S, Sandstrom DJ, Morton CC, Niedzwiecki CA, Sandstrom MM, Bieber FR. Prenat Diagn; 2001 Apr; 21(4):262-9. PubMed ID: 11288114 [Abstract] [Full Text] [Related]
8. Potential errors with rapid analysis techniques: partial duplication 21q resulting from a paternal paracentric insertion uncovered in chorionic villus sampling by fluorescence in situ hybridization. Ehrhardt N, Kujat A, Faber R, Horn LC, Froster UG. Fetal Diagn Ther; 2009 Apr; 26(4):219-22. PubMed ID: 20029221 [Abstract] [Full Text] [Related]
9. 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 [Abstract] [Full Text] [Related]
10. [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 Aug; 204(1):8-13. PubMed ID: 10721180 [Abstract] [Full Text] [Related]
11. [Prenatal diagnosis of common chromosomal aneuploidies on uncultured amniotic fluid cells by fluorescence in situ hybridization]. Xiao HM, Tan YQ, Li LY, Lu GX. Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Dec; 21(6):608-10. PubMed ID: 15583993 [Abstract] [Full Text] [Related]
12. Role of amniotic fluid interphase fluorescence in situ hybridization (FISH) analysis in patient management. Cheong Leung W, Chitayat D, Seaward G, Windrim R, Ryan G, Barrett J, Winsor EJ. Prenat Diagn; 2001 Apr; 21(4):327-32. PubMed ID: 11288128 [Abstract] [Full Text] [Related]
13. Detection of chromosomal abnormalities using fluorescence in situ hybridization (FISH). Jobanputra V, Kriplani A, Choudhry VP, Kucheria K. Natl Med J India; 1998 Apr; 11(6):259-63. PubMed ID: 10083791 [Abstract] [Full Text] [Related]
14. An assessment of the use of interphase FISH with chromosome specific probes as an alternative to cytogenetics in prenatal diagnosis. Thein AT, Abdel-Fattah SA, Kyle PM, Soothill PW. Prenat Diagn; 2000 Apr; 20(4):275-80. PubMed ID: 10740198 [Abstract] [Full Text] [Related]
15. 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 [Abstract] [Full Text] [Related]
16. 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 [Abstract] [Full Text] [Related]
17. [Rapid prenatal diagnosis of Down's syndrome in the first trimester of pregnancy by fluorescence in situ hybridization]. Xiang Y, Sun N, Wang F. Zhonghua Fu Chan Ke Za Zhi; 1997 Nov; 32(11):646-8. PubMed ID: 9639761 [Abstract] [Full Text] [Related]
18. [Rapid detection of numerical aberrations of chromosomes in the first trimester of pregnancy by using fluorescence in situ hybridization (FISH)]. Xiang Y, Bryndorf T, Philip J, Sun N. Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 1995 Apr; 17(2):120-4. PubMed ID: 7656391 [Abstract] [Full Text] [Related]
19. Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data. National Institute of Child Health and Development Fetal Cell Isolation Study. Bianchi DW, Simpson JL, Jackson LG, Elias S, Holzgreve W, Evans MI, Dukes KA, Sullivan LM, Klinger KW, Bischoff FZ, Hahn S, Johnson KL, Lewis D, Wapner RJ, de la Cruz F. Prenat Diagn; 2002 Jul; 22(7):609-15. PubMed ID: 12124698 [Abstract] [Full Text] [Related]
20. Advanced FISH with directly labeled X, Y and 18 DNA probes as a tool for rapid prenatal diagnosis. Aviram-Goldring A, Daniely M, Chaki R, Lipitz S, Barkai G, Goldman B. J Reprod Med; 1999 Jun; 44(6):497-503. PubMed ID: 10394543 [Abstract] [Full Text] [Related] Page: [Next] [New Search]