Fetal cell-free DNA fraction in maternal plasma is affected by fetal trisomy-Reference-Cited by-同舟云学术

Fetal cell-free DNA fraction in maternal plasma is affected by fetal trisomy

Published:2016-03-17 Issue:7 Volume:61 Page:647-652
ISSN:1434-5161
Container-title:Journal of Human Genetics
language:en
Short-container-title:J Hum Genet

Author:

Suzumori Nobuhiro, ,Ebara Takeshi,Yamada Takahiro,Samura Osamu,Yotsumoto Junko,Nishiyama Miyuki,Miura Kiyonori,Sawai Hideaki,Murotsuki Jun,Kitagawa Michihiro,Kamei Yoshimasa,Masuzaki Hideaki,Hirahara Fumiki,Saldivar Juan-Sebastian,Dharajiya Nilesh,Sago Haruhiko,Sekizawa Akihiko

Publisher

Springer Science and Business Media LLC

Subject

Genetics(clinical),Genetics

Link

http://www.nature.com/articles/jhg201625.pdf

Reference22 articles.

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2. Palomaki, G. E., Deciu, C., Kloza, E. M., Lambert-Messerlian, G. M., Haddow, J. E., Neveux, L. M. et al. DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study. Genet. Med. 14, 296–305 (2012).

3. Bianchi, D. W., Platt, L. D., Goldberg, J. D., Abuhamad, A. Z., Sehnert, A. J. & Rava, R. P. Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing. Maternal blood is source to accurately diagnose fetal aneuploidy (MELISSA) Study Group. Obstet. Gynecol. 119, 890–901 (2012).

4. Porreco, R. P., Garite, T. J., Maurel, K., Marusiak, B ., Obstetrix Collaborative Research Network, Ehrich, M. et al. Noninvasive prenatal screening for fetal trisomies 21, 18, 13 and the common sex chromosome aneuploidies from maternal blood using massively parallel genomic sequencing of DNA. Am. J. Obstet. Gynecol. 211, 365. e1–e12 (2014).

5. Norton, M. E., Jacobsson, B., Swamy, G. K., Laurent, L. C., Ranzini, A. C., Brar, H. et al. Cell-free DNA analysis for noninvasive examination of trisomy. N. Engl. J. Med. 372, 1589–1597 (2015).

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