308 related articles for article (PubMed ID: 18425471)
21. Prenatal detection of chromosome aneuploidy by quantitative fluorescence PCR.
Mann K; Petek E; Pertl B
Methods Mol Biol; 2008; 444():71-94. PubMed ID: 18425473
[TBL] [Abstract][Full Text] [Related]
22. Analysis of sperm aneuploidy by PRINS.
Pellestor F; Andréo B; Puechberty J; Lefort G; Sarda P
Methods Mol Biol; 2006; 334():49-59. PubMed ID: 16861752
[TBL] [Abstract][Full Text] [Related]
23. [From the conception of the PRINS to its coronation].
Krabchi K; Lavoie J; Coullin P; Bronsard M; Pellestor F; Yan J; Drouin R
Med Sci (Paris); 2004 Apr; 20(4):465-73. PubMed ID: 15124121
[TBL] [Abstract][Full Text] [Related]
24. 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]
25. Creating a new color by omission of 3 end blocking step for simultaneous detection of different chromosomes in multi-PRINS technique.
Yan J; Bronsard M; Drouin R
Chromosoma; 2001 Feb; 109(8):565-70. PubMed ID: 11305789
[TBL] [Abstract][Full Text] [Related]
26. Preimplantation genetic screening (PGS) in infertile female age > or = 35 years by fluorescence in situ hybridization of chromosome 13, 18, 21, X and Y.
Chiamchanya C; Visutakul P; Gumnarai N; Su-angkawatin W
J Med Assoc Thai; 2008 Nov; 91(11):1644-50. PubMed ID: 19127783
[TBL] [Abstract][Full Text] [Related]
27. Fast multicolor primed in situ protocol for chromosome identification in isolated cells may be used for human oocytes and polar bodies.
Pellestor F; Anahory T; Andréo B; Régnier-Vigouroux G; Soulié JP; Baudouin M; Demaille J
Fertil Steril; 2004 Feb; 81(2):408-15. PubMed ID: 14967382
[TBL] [Abstract][Full Text] [Related]
28. 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]
29. QF-PCR-based prenatal detection of aneuploidy in a southeast Asian population.
Quaife R; Wong LF; Tan SY; Chua WY; Lim SS; Hammersley CJ; Yeo HL
Prenat Diagn; 2004 Jun; 24(6):407-13. PubMed ID: 15229837
[TBL] [Abstract][Full Text] [Related]
30. [Use of the primed in situ labeling technique for a rapid detection of chromosomes X, 18].
Ni B; Li H; Zou Y; Wu S
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 1998 Dec; 15(6):373-5. PubMed ID: 9845772
[TBL] [Abstract][Full Text] [Related]
31. Detection of circulating fetal cells utilizing automated microscopy: potential for noninvasive prenatal diagnosis of chromosomal aneuploidies.
Seppo A; Frisova V; Ichetovkin I; Kim Y; Evans MI; Antsaklis A; Nicolaides KH; Tafas T; Tsipouras P; Kilpatrick MW
Prenat Diagn; 2008 Sep; 28(9):815-21. PubMed ID: 18646239
[TBL] [Abstract][Full Text] [Related]
32. Rapid prenatal diagnosis of aneuploidy using quantitative fluorescence-PCR (QF-PCR).
Ogilvie CM; Donaghue C; Fox SP; Docherty Z; Mann K
J Histochem Cytochem; 2005 Mar; 53(3):285-8. PubMed ID: 15750003
[TBL] [Abstract][Full Text] [Related]
33. Multicolor fluorescence in situ hybridization for the simultaneous detection of probe sets for chromosomes 13, 18, 21, X and Y in uncultured amniotic fluid cells.
Ried T; Landes G; Dackowski W; Klinger K; Ward DC
Hum Mol Genet; 1992 Aug; 1(5):307-13. PubMed ID: 1303206
[TBL] [Abstract][Full Text] [Related]
34. Rapid prenatal diagnosis of aneuploidies and zygosity in multiple pregnancies by amniocentesis with single insertion of the needle and quantitative fluorescent PCR.
Cirigliano V; Cañadas P; Plaja A; Ordoñez E; Mediano C; Sánchez A; Farrán I
Prenat Diagn; 2003 Aug; 23(8):629-33. PubMed ID: 12913868
[TBL] [Abstract][Full Text] [Related]
35. Prenatal detection of structural abnormalities of chromosome 18: associations with interphase fluorescence in situ hybridization (FISH) and maternal serum screening.
Graf MD; Gill P; Krew M; Schwartz S
Prenat Diagn; 2002 Aug; 22(8):645-8. PubMed ID: 12210569
[TBL] [Abstract][Full Text] [Related]
36. Direct detection of fetal cells in maternal blood: a reappraisal using a combination of two different Y chromosome-specific FISH probes and a single X chromosome-specific probe.
Babochkina T; Mergenthaler S; Dinges TM; Holzgreve W; Hahn S
Arch Gynecol Obstet; 2005 Dec; 273(3):166-9. PubMed ID: 16133462
[TBL] [Abstract][Full Text] [Related]
37. [Analysis of the frequency of spontaneous aneuploidy in human somatic cells using interphase cytogenetic technology].
Nazarenko SA; Timoshevskiĭ VA
Genetika; 2004 Feb; 40(2):195-204. PubMed ID: 15065426
[TBL] [Abstract][Full Text] [Related]
38. Correlation of abnormal rapid FISH and chromosome results from amniocytes for prenatal diagnosis.
Wyandt HE; Tonk VS; Huang XL; Evans AT; Milunsky JM; Milunsky A
Fetal Diagn Ther; 2006; 21(2):235-40. PubMed ID: 16491010
[TBL] [Abstract][Full Text] [Related]
39. Clinical applications of primed in situ labelling (PRINS) rapid identification of a marker chromosome in a fetus.
Velagaleti GV; Carpenter NJ; Tharapel AT
Ann Genet; 1997; 40(3):154-7. PubMed ID: 9401104
[TBL] [Abstract][Full Text] [Related]
40. Routine prenatal diagnosis of aneuploidy by FISH studies in high-risk pregnancies.
Feldman B; Ebrahim SA; Hazan SL; Gyi K; Johnson MP; Johnson A; Evans MI
Am J Med Genet; 2000 Jan; 90(3):233-8. PubMed ID: 10678661
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]