158 related articles for article (PubMed ID: 10416971)
21. [Quick prenatal diagnosis using FISH in the analysis of non-cultured amniotic fluid cells].
Marguerat P; Gaide AC; Thonney F; Schorderet D
Rev Med Suisse Romande; 2000 May; 120(5):401-7. PubMed ID: 10911743
[TBL] [Abstract][Full Text] [Related]
22. [Analysis of 89 amniotic samples using fluorescent in situ hybridization].
Wei P; Li YX; Zeng L; Chen C; Qin SF; Wang XY; Xi N; Tang SQ; Leng M; Liu CL
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Apr; 30(2):214-7. PubMed ID: 23568739
[TBL] [Abstract][Full Text] [Related]
23. Prenatal diagnosis from cystic hygroma fluid: the value of fluorescence in situ hybridization.
Donnenfeld AE; Lockwood D; Lamb AN
Am J Obstet Gynecol; 2001 Oct; 185(4):1004-8. PubMed ID: 11641692
[TBL] [Abstract][Full Text] [Related]
24. Rapid detection of chromosomal aneuploidies in uncultured amniocytes by multiplex ligation-dependent probe amplification (MLPA).
Hochstenbach R; Meijer J; van de Brug J; Vossebeld-Hoff I; Jansen R; van der Luijt RB; Sinke RJ; Page-Christiaens GC; Ploos van Amstel JK; de Pater JM
Prenat Diagn; 2005 Nov; 25(11):1032-9. PubMed ID: 16231311
[TBL] [Abstract][Full Text] [Related]
25. [Identification of aneuploids in uncultured amniotic fluid cells by interphase fluorescence in situ hybridization].
Sohda M; Harada N; Nishimura T; Noda K; Abe K; Niikawa N
Rinsho Byori; 1998 May; 46(5):486-92. PubMed ID: 9627501
[TBL] [Abstract][Full Text] [Related]
26. Comparison of comparative genomic hybridization with conventional karyotype and classical fluorescence in situ hybridization for prenatal and postnatal diagnosis of unbalanced chromosome abnormalities.
Lapierre JM; Cacheux V; Collot N; Da Silva F; Hervy N; Rivet D; Romana S; Wiss J; Benzaken B; Aurias A; Tachdjian G
Ann Genet; 1998; 41(3):133-40. PubMed ID: 9833066
[TBL] [Abstract][Full Text] [Related]
27. 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]
28. 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
[TBL] [Abstract][Full Text] [Related]
29. Detection of mosaicism for primary trisomies in prenatal samples by QF-PCR and karyotype analysis.
Donaghue C; Mann K; Docherty Z; Ogilvie CM
Prenat Diagn; 2005 Jan; 25(1):65-72. PubMed ID: 15662691
[TBL] [Abstract][Full Text] [Related]
30. Rapid detection of selected aneuploidies by quantitative fluorescent PCR.
Adinolfi M; Sherlock J; Pertl B
Bioessays; 1995 Jul; 17(7):661-4. PubMed ID: 7646488
[TBL] [Abstract][Full Text] [Related]
31. 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]
32. [Rapid detection of 18-trisomy syndrome using primed in situ labeling technique].
Yang JB; Zheng S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Feb; 21(1):74-6. PubMed ID: 14767916
[TBL] [Abstract][Full Text] [Related]
33. Role of multicolor fluorescence in situ hybridization (FISH) in simultaneous detection of probe sets for chromosome 18, X and Y in uncultured amniotic fluid cells.
Kim JI; Rhee JH
J Korean Med Sci; 1999 Aug; 14(4):438-42. PubMed ID: 10485625
[TBL] [Abstract][Full Text] [Related]
34. [Application of combined fluorescence in situ hybridization and karyotype analysis for the diagnosis of Robertsonian translocation type trisomy 21].
Zhang WG; Zhang WQ; Dai MZ; Chen XJ; Zhang Y; Zheng R
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2013 Apr; 30(2):210-3. PubMed ID: 23568738
[TBL] [Abstract][Full Text] [Related]
35. 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
[TBL] [Abstract][Full Text] [Related]
36. 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]
37. [Optimized procedure for fluorescence in situ hybridization in rapid prenatal diagnosis of common aneuploidy].
Wu J; Zhong M; Lu J; Pan XY; Guo L; Wang T
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2011 Dec; 28(6):658-60. PubMed ID: 22161099
[TBL] [Abstract][Full Text] [Related]
38. Real-time quantitative PCR for the detection of fetal aneuploidies.
Zimmermann BG; Dudarewicz L
Methods Mol Biol; 2008; 444():95-109. PubMed ID: 18425474
[TBL] [Abstract][Full Text] [Related]
39. Fully automated FISH examination of amniotic fluid cells.
Wauters J; Assche EV; Antsaklis A; Tepperberg J; Sharp SM; Kilpatrick MW; Tafas T; Tsipouras P
Prenat Diagn; 2007 Oct; 27(10):951-5. PubMed ID: 17602444
[TBL] [Abstract][Full Text] [Related]
40. 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]
[Previous] [Next] [New Search]
