Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21-Reference-Cited by-同舟云学术

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Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21

Published:2011-03-06 Issue:4 Volume:17 Page:510-513
ISSN:1078-8956
Container-title:Nature Medicine
language:en
Short-container-title:Nat Med

Author:

Papageorgiou Elisavet A,Karagrigoriou Alex,Tsaliki Evdokia,Velissariou Voula,Carter Nigel P,Patsalis Philippos C

Publisher

Springer Science and Business Media LLC

Subject

General Biochemistry, Genetics and Molecular Biology,General Medicine

Link

http://www.nature.com/articles/nm.2312.pdf

Reference27 articles.

1. Hultén, M.A., Dhanjal, S. & Pertl, B. Rapid and simple prenatal diagnosis of common chromosome disorders: advantages and disadvantages of the molecular methods FISH and QF-PCR. Reproduction 126, 279–297 (2003).

2. Lo, Y.M. et al. Presence of fetal DNA in maternal plasma and serum. Lancet 350, 485–487 (1997).

3. Honda, H. et al. Fetal gender determination in early pregnancy through qualitative and quantitative analysis of fetal DNA in maternal serum. Hum. Genet. 110, 75–79 (2002).

4. Bianchi, D.W., Avent, N.D., Costa, J.M. & van der Schoot, C.E. Noninvasive prenatal diagnosis of fetal Rhesus D: ready for prime(r) time. Obstet. Gynecol. 106, 841–844 (2005).

5. Lo, Y.M. et al. Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma. N. Engl. J. Med. 339, 1734–1738 (1998).

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