210 related articles for article (PubMed ID: 16862671)
1. Chromosome analysis of uncultured amniocytes by comparative genomic hybridization in early amniocentesis.
Ketupanya A; Aranyakasemsuk N; Tocharoentanaphol C; Vuthiwong C
J Med Assoc Thai; 2005 Nov; 88 Suppl 3():S1-6. PubMed ID: 16862671
[TBL] [Abstract][Full Text] [Related]
2. Analysis of uncultured amniocytes by comparative genomic hybridization: a prospective prenatal study.
Lapierre JM; Cacheux V; Luton D; Collot N; Oury JF; Aurias A; Tachdjian G
Prenat Diagn; 2000 Feb; 20(2):123-31. PubMed ID: 10694684
[TBL] [Abstract][Full Text] [Related]
3. Comparative genomic hybridization-assisted prenatal diagnosis of a de novo inverted duplication of chromosome 10q. A case report.
Chen CK; Chang SD; Chen YJ; Hsueh DW; Soong YK
J Reprod Med; 2003 May; 48(5):391-4. PubMed ID: 12815917
[TBL] [Abstract][Full Text] [Related]
4. Rapid prenatal diagnosis using uncultured amniocytes and oligonucleotide array CGH.
Bi W; Breman AM; Venable SF; Eng PA; Sahoo T; Lu XY; Patel A; Beaudet AL; Cheung SW; White LD
Prenat Diagn; 2008 Oct; 28(10):943-9. PubMed ID: 18792925
[TBL] [Abstract][Full Text] [Related]
5. Rapid positive confirmation of mosaicism for a small supernumerary marker chromosome as r(8) by interphase fluorescence in situ hybridization, quantitative fluorescent polymerase chain reaction, and array comparative genomic hybridization on uncultured amniocytes in a pregnancy with fetal pyelectasis.
Chen CP; Chang SD; Su YN; Chen M; Chern SR; Su JW; Chen YT; Chen WL; Pan CW; Lee MS; Wang W
Taiwan J Obstet Gynecol; 2012 Sep; 51(3):405-10. PubMed ID: 23040926
[TBL] [Abstract][Full Text] [Related]
6. 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]
7. Prenatal diagnosis of a de novo supernumerary marker chromosome originating from chromosome 16.
Yakut S; Cetin Z; Simşek M; Karaüzüm SB; Tükün A; Lüleci G
Genet Couns; 2009; 20(4):327-32. PubMed ID: 20162867
[TBL] [Abstract][Full Text] [Related]
8. [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]
9. FastFISH: technique for ultrarapid fluorescence in situ hybridization on uncultured amniocytes yielding results within 2 h of amniocentesis.
Choolani M; Ho SS; Razvi K; Ponnusamy S; Baig S; Fisk NM; Biswas A;
Mol Hum Reprod; 2007 Jun; 13(6):355-9. PubMed ID: 17430982
[TBL] [Abstract][Full Text] [Related]
10. [Application of the fluorescent in situ hybridization on the prenatal diagnosis of the fetal aneuploidy in the uncultured amniocytes].
Qi Q; Sun N; Hao N
Zhonghua Fu Chan Ke Za Zhi; 2000 Sep; 35(9):517-9. PubMed ID: 11775938
[TBL] [Abstract][Full Text] [Related]
11. [Two different genetic analyses of spontaneously aborted specimen].
Hu YL; Chen X; Chen LL; Zhu RF; Xu ZF; Wang ZQ; Zhu XH; Liu X
Zhonghua Fu Chan Ke Za Zhi; 2006 Mar; 41(3):148-51. PubMed ID: 16640875
[TBL] [Abstract][Full Text] [Related]
12. [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]
13. 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
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. [Rapid prenatal diagnosis of chromosome aneuploidies in 60 uncultured amniotic fluid samples by fluorescence in situ hybridization].
Wang H; Li H; Wang H; Wang H; Xia Y; Wen J; Long Z; Dai H; Liang D; Xia J; Wu L
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2008 Oct; 25(5):538-41. PubMed ID: 18841567
[TBL] [Abstract][Full Text] [Related]
16. [Application of fluorescence in situ hybridization in prenatal diagnosis of chromosomal abnormalities in uncultured amniocytes: a multi-center study].
Wang SY; Huang XH; Jia CW; Li Y; Ren GQ
Zhonghua Fu Chan Ke Za Zhi; 2009 Jul; 44(7):492-5. PubMed ID: 19957546
[No Abstract] [Full Text] [Related]
17. Pitfalls in prenatal diagnosis: cytogenetic analysis in amniocytes fails to detect mosaic r(12).
de Pater JM; Scheres JM; Christiaens GC; Ausems MG
Prenat Diagn; 2003 Jan; 23(1):65-7. PubMed ID: 12533816
[TBL] [Abstract][Full Text] [Related]
18. [The application and significance in prenatal diagnosis using G-banding, fluorescence in situ hybridization and comparative genomic hybridization].
Zhang WS; Chen QN; Wu XH; Liang QH
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2009 Apr; 26(2):156-60. PubMed ID: 19350506
[TBL] [Abstract][Full Text] [Related]
19. Detection of trisomy 21 by quantitative fluorescent-polymerase chain reaction in uncultured amniocytes.
Solassol J; Rahil H; Sapin V; Lemery D; Dastugue B; Boespflug-Tanguy O; Creveaux I
Prenat Diagn; 2003 Apr; 23(4):287-91. PubMed ID: 12673631
[TBL] [Abstract][Full Text] [Related]
20. Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH)-Re-evaluation of chromosome aberration rates in early spontaneous abortions.
Fritz B; Hallermann C; Olert J; Fuchs B; Bruns M; Aslan M; Schmidt S; Coerdt W; Müntefering H; Rehder H
Eur J Hum Genet; 2001 Jul; 9(7):539-47. PubMed ID: 11464246
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
