Portal de Periódicos da CAPES

Response to ”concerns about the statistical methodology described in the ‘Clinical application of massively parallel sequencing‐based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11 105 pregnancies with mixed risk factors’”

2013; Wiley; Volume: 33; Issue: 13 Linguagem: Inglês

10.1002/pd.4261

1097-0223

Wei Wang,

Parvovirus B19 Infection Studies

Prenatal DiagnosisVolume 33, Issue 13 p. 1314-1315 Correspondence Response to ”concerns about the statistical methodology described in the ‘Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11 105 pregnancies with mixed risk factors’” Wei Wang, Corresponding Author Wei Wang BGI-Shenzhen, Shenzhen, ChinaCorrespondence to: Wei Wang. E-mail: [email protected]Search for more papers by this author Wei Wang, Corresponding Author Wei Wang BGI-Shenzhen, Shenzhen, ChinaCorrespondence to: Wei Wang. E-mail: [email protected]Search for more papers by this author First published: 10 December 2013 https://doi.org/10.1002/pd.4261Citations: 1 Funding sources: None Conflicts of interest: None declared Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat No abstract is available for this article. REFERENCES 1 Dan S, Wang W, Ren J et al. Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factors. Prenat Diagn 2012; 32(13): 1225–32. 2 Jiang F, Ren J, Chen F et al. Noninvasive fetal trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies. BMC Med Genomics 2012; 5: 57. 3 Chen S, Lau TK, Zhang C et al. A method for noninvasive detection of fetal large deletions/duplications by low coverage massively parallel sequencing. Prenat Diagn 2013; 33(6): 584–90. Citing Literature Volume33, Issue13December 2013Pages 1314-1315 ReferencesRelatedInformation