263 related articles for article (PubMed ID: 7656391)
1. [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
[TBL] [Abstract][Full Text] [Related]
2. [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
[TBL] [Abstract][Full Text] [Related]
3. [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
[TBL] [Abstract][Full Text] [Related]
4. 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
[TBL] [Abstract][Full Text] [Related]
5. [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; 200(5):186-90. PubMed ID: 9035828
[TBL] [Abstract][Full Text] [Related]
6. [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]
7. Rapid detection of numerical aberrations of chromosomes 13, 18 and 21 in chorionic mesenchymal cells.
Bryndorf T; Christensen B; Xiang Y; Lind AM; Philip J
Prenat Diagn; 1993 Sep; 13(9):815-23. PubMed ID: 8278312
[TBL] [Abstract][Full Text] [Related]
8. Chromosomal changes detected by fluorescence in situ hybridization in patients with acute lymphoblastic leukemia.
Zhang L; Parkhurst JB; Kern WF; Scott KV; Niccum D; Mulvihill JJ; Li S
Chin Med J (Engl); 2003 Sep; 116(9):1298-303. PubMed ID: 14527352
[TBL] [Abstract][Full Text] [Related]
9. Detection of chromosomal abnormalities using fluorescence in situ hybridization (FISH).
Jobanputra V; Kriplani A; Choudhry VP; Kucheria K
Natl Med J India; 1998; 11(6):259-63. PubMed ID: 10083791
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Two years' prospective experience using fluorescence in situ hybridization on uncultured amniotic fluid cells for rapid prenatal diagnosis of common chromosomal aneuploidies.
Morris A; Boyd E; Dhanjal S; Lowther GW; Aitken DA; Young J; Menzies AL; Imrie SJ; Connor JM
Prenat Diagn; 1999 Jun; 19(6):546-51. PubMed ID: 10416971
[TBL] [Abstract][Full Text] [Related]
12. Prenatal diagnosis with repetitive in situ hybridization probes.
Lebo RV; Flandermeyer RR; Diukman R; Lynch ED; Lepercq JA; Golbus MS
Am J Med Genet; 1992 Jul; 43(5):848-54. PubMed ID: 1642274
[TBL] [Abstract][Full Text] [Related]
13. 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]
14. [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; 36(2):76-8. PubMed ID: 11783350
[TBL] [Abstract][Full Text] [Related]
15. 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]
16. 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; 26(4):219-22. PubMed ID: 20029221
[TBL] [Abstract][Full Text] [Related]
17. 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
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. [Application of fluorescence in situ hybridization to prenatal diagnosis of aneuploidy in 110 uncultured amniotic fluid samples].
Liu H; Liao C; Huang YN; Pan M; Yi CX; Yuan SM; Hu SY; Zhong HZ
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2010 Aug; 27(4):453-6. PubMed ID: 20677157
[TBL] [Abstract][Full Text] [Related]
20. Prenatal detection of Down's syndrome by rapid aneuploidy testing for chromosomes 13, 18, and 21 by FISH or PCR without a full karyotype: a cytogenetic risk assessment.
Caine A; Maltby AE; Parkin CA; Waters JJ; Crolla JA;
Lancet; 2005 Jul 9-15; 366(9480):123-8. PubMed ID: 16005334
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]