134 related articles for article (PubMed ID: 17697586)
1. Prenatal diagnosis of nonmosaic tetrasomy 9p by microdissection and FISH: case report.
Tan YQ; Chen XM; Hu L; Guan XY; Lu GX
Chin Med J (Engl); 2007 Jul; 120(14):1281-3. PubMed ID: 17697586
[No Abstract] [Full Text] [Related]
2. 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]
3. Increased efficiency of fluorescence in situ hybridization (FISH) using the microwave.
Weise A; Liehr T; Claussen U; Halbhuber KJ
J Histochem Cytochem; 2005 Oct; 53(10):1301-3. PubMed ID: 15923358
[TBL] [Abstract][Full Text] [Related]
4. 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]
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. [Application of spectral karyotyping in diagnosis and prenatal diagnosis of the marker chromosome].
Liao C; Pan M; Li DZ; Yi CX; Hu SY; Yuan SM; Wu SQ
Zhonghua Fu Chan Ke Za Zhi; 2008 May; 43(5):321-4. PubMed ID: 18953861
[TBL] [Abstract][Full Text] [Related]
7. [Fluorescent in situ hybridization (FISH). A new dimension of genetics].
Blennow ES
Lakartidningen; 1994 Oct; 91(43):3901-5. PubMed ID: 7967959
[No Abstract] [Full Text] [Related]
8. 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]
9. [Rapid prenatal diagnosis of chromosome abnormalities: from FISH to QF-PCR].
Conrad B; Bena F; Dahoun-Hadorn S
Rev Med Suisse; 2005 Mar; 1(11):785-8. PubMed ID: 15856851
[TBL] [Abstract][Full Text] [Related]
10. Euchromatic variant 16p+. Implications in prenatal diagnosis.
López Pajares I; Villa O; Salido M; Mori MA; Gonzalez A; Lapunzina P; De Torres ML; Vallcorba I; Palomares M; Fernández L; Delicado A
Prenat Diagn; 2006 Jun; 26(6):535-8. PubMed ID: 16634122
[TBL] [Abstract][Full Text] [Related]
11. Prenatal diagnosis of chromosomal abnormalities using maternal blood.
Bischoff FZ; Dang DX; Lewis DE; Simpson JL
Methods Mol Biol; 2002; 204():243-58. PubMed ID: 12397802
[No Abstract] [Full Text] [Related]
12. High-density array comparative genomic hybridization analysis and follow-up of a child with a de novo complex chromosome rearrangement detected prenatally.
Quadrelli A; Vaglio A; Quadrelli R; Mechoso B; Fan YS; Huang T
Prenat Diagn; 2007 Oct; 27(10):982-3. PubMed ID: 17899566
[No Abstract] [Full Text] [Related]
13. [A new rapid test (FISH) for the prenatal diagnosis of the most frequent chromosome aberrations--what significance has it in practice?].
Eiben B; Hammans W; Goebel R; Epplen JT
Dtsch Med Wochenschr; 1998 Jan; 123(3):55-7. PubMed ID: 9472221
[No Abstract] [Full Text] [Related]
14. Characterization of marker chromosomes by microdissection and fluorescence in situ hybridization.
Thangavelu M; Pergament E; Espinosa R; Bohlander SK
Prenat Diagn; 1994 Jul; 14(7):583-8. PubMed ID: 7971760
[TBL] [Abstract][Full Text] [Related]
15. Rapid prenatal diagnosis of trisomies 13, 18, 21 and sex chromosome anomalies by fluorescence in situ hybridization: a year's experience.
Li S; Stanley JR; Draper ML; Mirabile CP; Coleman FH; Mulvihill JJ
J Okla State Med Assoc; 2002 Apr; 95(4):244-6. PubMed ID: 11957840
[TBL] [Abstract][Full Text] [Related]
16. [Preimplantation genetic diagnosis using the FISH technic].
Plachot M
Contracept Fertil Sex; 1999; 27(7-8):491-4. PubMed ID: 10495565
[No Abstract] [Full Text] [Related]
17. Rapid prenatal diagnosis of chromosome abnormalities.
Tan SY; Chan WB; Cheng WC; Hagarty A; Lim KT; Quaife R
Singapore Med J; 2000 Oct; 41(10):493-7. PubMed ID: 11281441
[TBL] [Abstract][Full Text] [Related]
18. 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]
19. Genetic Testing: from chromosomes to DNA, a revolution in prenatal diagnosis.
Breuning MH
Eur J Hum Genet; 2005 May; 13(5):517-8. PubMed ID: 15726111
[No Abstract] [Full Text] [Related]
20. [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]
[Next] [New Search]