235 related articles for article (PubMed ID: 17715994)
21. The detection of aneuploidy and maternal contamination by QF-PCR in samples undergoing prenatal diagnosis for thalassemia in Southern China.
Liao C; Yang X; Li FT; Li J; Li DZ
Eur J Obstet Gynecol Reprod Biol; 2009 Jun; 144(2):149-52. PubMed ID: 19375212
[TBL] [Abstract][Full Text] [Related]
22. Double aneuploidy (48,XXY,+21) of maternal origin in a child born to a 13-year-old mother: evaluation of the maternal folate metabolism.
Biselli JM; Machado FB; Zampieri BL; Alves da Silva AF; Goloni-Bertollo EM; Haddad R; Eberlin MN; Vannucchi H; Carvalho VM; Medina-Acosta E; Pavarino-Bertelli EC
Genet Couns; 2009; 20(3):225-34. PubMed ID: 19852428
[TBL] [Abstract][Full Text] [Related]
23. Diagnosis of Down syndrome and detection of origin of nondisjunction by short tandem repeat analysis.
Jain S; Agarwal S; Panigrahi I; Tamhankar P; Phadke S
Genet Test Mol Biomarkers; 2010 Aug; 14(4):489-91. PubMed ID: 20722466
[TBL] [Abstract][Full Text] [Related]
24. A prospective study on the effect of rapid aneuploidy testing (amnio-PCR) on anxiety levels and quality of life measures in women and their partners with positive Down screening result.
Leung WC; Lau ET; Ngai C; Lam H; Leung KY; Lee CP; Lao TT; Tang MH
Fetal Diagn Ther; 2008; 24(3):165-9. PubMed ID: 18753751
[TBL] [Abstract][Full Text] [Related]
25. Noninvasive prenatal diagnosis of aneuploidy using cell-free nucleic acids in maternal blood: promises and unanswered questions.
Puszyk WM; Crea F; Old RW
Prenat Diagn; 2008 Jan; 28(1):1-6. PubMed ID: 18022821
[TBL] [Abstract][Full Text] [Related]
26. [Rapid diagnosis of 21 trisomy syndrome by fluorescence quantitative polymerase chain reaction].
Jing CX; Xie XZ; Zhang Q; Lan D
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2004 Aug; 21(4):398-9. PubMed ID: 15300645
[TBL] [Abstract][Full Text] [Related]
27. To err (meiotically) is human: the genesis of human aneuploidy.
Hassold T; Hunt P
Nat Rev Genet; 2001 Apr; 2(4):280-91. PubMed ID: 11283700
[TBL] [Abstract][Full Text] [Related]
28. Identification of X chromosome copies by quantitative real-time polymerase chain reaction for population screening tests.
Ramos ES; Serafim JV; Takeuchi PL; Marcondes CR; Araújo A
Fertil Steril; 2010 Nov; 94(6):2476-8. PubMed ID: 20493475
[TBL] [Abstract][Full Text] [Related]
29. MLPA for prenatal diagnosis of commonly occurring aneuploidies.
Schouten J; Galjaard RJ
Methods Mol Biol; 2008; 444():111-22. PubMed ID: 18425475
[TBL] [Abstract][Full Text] [Related]
30. Quantitative fluorescent-polymerase chain reaction: first line investigation for trisomy 21 in a developing country.
Gulati R; Muthuswamy S; Bhat VB; Agarwal S
J Paediatr Child Health; 2014 Aug; 50(8):656-7. PubMed ID: 25080985
[No Abstract] [Full Text] [Related]
31. Molecular methods for rapid detection of aneuploidy.
Dudarewicz L; Holzgreve W; Jeziorowska A; Jakubowski L; Zimmermann B
J Appl Genet; 2005; 46(2):207-15. PubMed ID: 15876689
[TBL] [Abstract][Full Text] [Related]
32. Rapid prenatal diagnosis of common chromosome aneuploidies by QF-PCR, results of 9 years of clinical experience.
Cirigliano V; Voglino G; Ordoñez E; Marongiu A; Paz Cañadas M; Ejarque M; Rueda L; Lloveras E; Fuster C; Adinolfi M
Prenat Diagn; 2009 Jan; 29(1):40-9. PubMed ID: 19173345
[TBL] [Abstract][Full Text] [Related]
33. Rapid prenatal diagnosis of trisomy 21 by fluorescent quantitative multiplex polymerase chain reaction.
Zheng F; Zhou X; Zhang YZ; Sun XB; Peng JH; Wang CH; Xiong CL; Li X
Chin Med J (Engl); 2006 Mar; 119(6):514-7. PubMed ID: 16584651
[No Abstract] [Full Text] [Related]
34. 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]
35. [Three-dimensional scatter plot analysis to estimate the risk of foetal aneuloidy].
Schmidt P; Hörmansdörfer C; Oehler K; Härtel H; Hillemanns P; Scharf A
Z Geburtshilfe Neonatol; 2008 Aug; 212(4):127-35. PubMed ID: 18729035
[TBL] [Abstract][Full Text] [Related]
36. QF-PCR for prenatal diagnosis of common aneuploides in women of advanced maternal age.
Lampret J; Lane T; Christianson A
S Afr Med J; 2008 Feb; 98(2):68-9. PubMed ID: 18350189
[No Abstract] [Full Text] [Related]
37. Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood.
Fan HC; Blumenfeld YJ; Chitkara U; Hudgins L; Quake SR
Proc Natl Acad Sci U S A; 2008 Oct; 105(42):16266-71. PubMed ID: 18838674
[TBL] [Abstract][Full Text] [Related]
38. OmniPlex--a new QF-PCR assay for prenatal diagnosis of common aneuploidies based on evaluation of the heterozygosity of short tandem repeat loci in the Czech population.
Putzova M; Pecnova L; Dvorakova L; Soldatova I; Goetz P; Stejskal D
Prenat Diagn; 2008 Dec; 28(13):1214-20. PubMed ID: 19012274
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. No beneficial effect of preimplantation genetic screening in women of advanced maternal age with a high risk for embryonic aneuploidy.
Twisk M; Mastenbroek S; Hoek A; Heineman MJ; van der Veen F; Bossuyt PM; Repping S; Korevaar JC
Hum Reprod; 2008 Dec; 23(12):2813-7. PubMed ID: 18567895
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]