114 related articles for article (PubMed ID: 20029221)
1. 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]
2. 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]
3. 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]
4. [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]
5. [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]
6. 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]
7. 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]
8. Prenatal detection of isochromosome 21 by QF-PCR. A comparison between FISH and traditional karyotyping.
Gole L; Lian NB; Lian NP; Rauff M; Biswas A; Choolani M
Fetal Diagn Ther; 2008; 24(1):47-50. PubMed ID: 18504381
[TBL] [Abstract][Full Text] [Related]
9. Minute chromosomal rearrangements detected prenatally by fluorescence in situ hybridization.
Suzumori K; Tanemura M; Oya N; Suzumori N; Kim KC; Ohashi H; Fukushima Y
Prenat Diagn; 1998 Jul; 18(7):725-30. PubMed ID: 9706655
[TBL] [Abstract][Full Text] [Related]
10. 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]
11. Prenatal diagnosis of partial monosomy 18p(18p11.2-->pter) and trisomy 21q(21q22.3-->qter) with alobar holoprosencephaly and premaxillary agenesis.
Chen CP; Chern SR; Wang W; Lee CC; Chen WL; Chen LF; Chang TY; Tzen CY
Prenat Diagn; 2001 May; 21(5):346-50. PubMed ID: 11360273
[TBL] [Abstract][Full Text] [Related]
12. 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]
13. [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]
14. Maternal balanced translocation (4;21) leading to an offspring with partial duplication of 4q and 21q without phenotypic manifestations of Down syndrome.
El-Ruby M; Hemly NA; Zaki MS
Genet Couns; 2007; 18(2):217-26. PubMed ID: 17710874
[TBL] [Abstract][Full Text] [Related]
15. Prenatal diagnosis of a fetus affected with Down syndrome and deletion 1p36 syndrome by fluorescence in situ hybridization and spectral karyotyping.
Hsieh LJ; Hsieh TC; Yeh GP; Lin MI; Chen M; Wang BB
Fetal Diagn Ther; 2004; 19(4):356-60. PubMed ID: 15192296
[TBL] [Abstract][Full Text] [Related]
16. [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]
17. [Application of fluorescence in situ hybridization to prenatal diagnosis of Down syndrome].
Wang M; Li QF; Qiao FY
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2005 Jun; 22(3):317-9. PubMed ID: 15952125
[TBL] [Abstract][Full Text] [Related]
18. Investigation of bone marrow involvement in malignant lymphoma using fluorescence in situ hybridization: possible utility in the detection of micrometastasis.
Huh HJ; Min HC; Cho HI; Chae SL; Lee DS
Cancer Genet Cytogenet; 2008 Oct; 186(1):1-5. PubMed ID: 18786435
[TBL] [Abstract][Full Text] [Related]
19. Interphase fluorescence in situ hybridization in a Turner syndrome variant with IsoXq. A case report.
Chang SD; Lin SL; Chen FP; Chu KK
J Reprod Med; 1996 Mar; 41(3):175-8. PubMed ID: 8778416
[TBL] [Abstract][Full Text] [Related]
20. 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]
[Next] [New Search]
