190 related articles for article (PubMed ID: 18598216)
1. Fluorescence in situ hybridization for prenatal screening of chromosomal aneuploidies.
Weise A; Liehr T
Expert Rev Mol Diagn; 2008 Jul; 8(4):355-7. PubMed ID: 18598216
[No Abstract] [Full Text] [Related]
2. Fluorescence in situ hybridization in prenatal screening: lessons from an inherited chromosome 18 marker.
Valentin M; Ottenwalter A; Serero S; Muller F; Luton D; Ducarme G
Prenat Diagn; 2009 Dec; 29(12):1177-9. PubMed ID: 19816880
[No Abstract] [Full Text] [Related]
3. 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]
4. 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]
5. [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]
6. False-positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha-satellite DNA probe (D18Z1) to the heterochromatic region of chromosome 9.
Wei S; Siu VM; Decker A; Quigg MH; Roberson J; Xu J; Adeyinka A
Prenat Diagn; 2007 Nov; 27(11):1064-6. PubMed ID: 17654752
[No Abstract] [Full Text] [Related]
7. Spectral karyotyping, fluorescence in situ hybridization and molecular genetic analysis of de novo partial trisomy 7p (7p15.1 --> pter) and partial monosomy 9p (9p22 --> pter).
Chen CP; Lin SP; Lin CC; Li YC; Hsieh LJ; Chern SR; Lee CC; Chen YJ; Wang W
Prenat Diagn; 2005 Dec; 25(12):1170-2. PubMed ID: 16315335
[No Abstract] [Full Text] [Related]
8. [Confirmation of a prenatal diagnosis of trisomy 13 with comparative genomic hybridization (CGH)].
Marton T; Thein A; Bán Z; Soothill P; Oroszné NJ; Papp Z
Orv Hetil; 2001 May; 142(19):997-1000. PubMed ID: 11419300
[TBL] [Abstract][Full Text] [Related]
9. [Establishment of multiple quantitative fluorescent polymerase chain reaction assay and its application in rapid prenatal diagnosis of common chromosome aneuploidies].
Xu AQ; Bian XM; Liu JT; Yao FX; Zhang WM; Hao N; Zhou J
Zhonghua Fu Chan Ke Za Zhi; 2010 Jul; 45(7):481-7. PubMed ID: 21029597
[TBL] [Abstract][Full Text] [Related]
10. Application of interphase FISH to uncultured amniocytes for rapid confirmation of true trisomy 2 mosaicism in the case of suspected amniocyte mosaicism involving trisomy 2 in a single colony.
Chen CP; Hung FY; Chern SR; Wu PS; Su JW; Wang W
Taiwan J Obstet Gynecol; 2013 Jun; 52(2):300-2. PubMed ID: 23915872
[No Abstract] [Full Text] [Related]
11. [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]
12. Optimized criteria for using fluorescence in situ hybridization in the prenatal diagnosis of common aneuploidies.
Leclercq S; Lebbar A; Grange G; Tsatsaris V; Le Tessier D; Dupont JM
Prenat Diagn; 2008 Apr; 28(4):313-8. PubMed ID: 18306148
[TBL] [Abstract][Full Text] [Related]
13. Prenatal diagnosis of complete sole trisomy 1q.
Pettenati MJ; Berry M; Shashi V; Hartley Bowen J; Harper M
Prenat Diagn; 2001 Jun; 21(6):435-40. PubMed ID: 11438944
[TBL] [Abstract][Full Text] [Related]
14. Rapid prenatal aneuploidy screening by fluorescence in situ hybridization (FISH).
Weise A; Liehr T
Methods Mol Biol; 2008; 444():39-47. PubMed ID: 18425470
[TBL] [Abstract][Full Text] [Related]
15. [A case of 18-trisomy diagnosed by fluorescence in situ hybridization of amniocyte].
Maruyama H; Fukushi Y; Tando T; Wada J; Niino T; Sato S; Kagiya A; Sato S; Saito Y
Nihon Sanka Fujinka Gakkai Zasshi; 1994 Jul; 46(7):611-3. PubMed ID: 8089600
[No Abstract] [Full Text] [Related]
16. Fetoplacental and fetoamniotic chromosomal discrepancies in prenatally detected mosaic trisomy 9.
Chen CP; Chern SR; Town DD; Wang W; Liao YW
Prenat Diagn; 2003 Dec; 23(12):1019-21. PubMed ID: 14663842
[No Abstract] [Full Text] [Related]
17. [The preimplantation diagnosis of genetic defects].
Delimitreva SM; Zhivkova RS; Vatev ITs
Akush Ginekol (Sofiia); 1996; 35(4):25-7. PubMed ID: 9254563
[No Abstract] [Full Text] [Related]
18. [Detection of chromosomal aneuploidies in fetus by multiplex Q-PCR method].
Helszer Z; Nowacka J; Kałuzewski B
Ginekol Pol; 2002 May; 73(5):444-8. PubMed ID: 12185705
[TBL] [Abstract][Full Text] [Related]
19. Resolution of trisomic mosaicism in prenatal diagnosis: estimated performance of a 50K SNP microarray.
Cross J; Peters G; Wu Z; Brohede J; Hannan GN
Prenat Diagn; 2007 Dec; 27(13):1197-204. PubMed ID: 17994637
[TBL] [Abstract][Full Text] [Related]
20. Rapid prenatal diagnosis of common aneuploidies in amniotic fluid using quantitative fluorescent polymerase chain reaction.
Onay H; Ugurlu T; Aykut A; Pehlivan S; Inal M; Tinar S; Ozkinay C; Ozkinay F
Gynecol Obstet Invest; 2008; 66(2):104-10. PubMed ID: 18446039
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
