Molecular detection of CFFDNA for early laboratory diagnosis of X linked disorders carriers-Reference-Cited by-同舟云学术

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Molecular detection of CFFDNA for early laboratory diagnosis of X linked disorders carriers

Published:2017-12 Issue:4 Volume:22 Page:260-263
ISSN:1110-5690
Container-title:Middle East Fertility Society Journal
language:en
Short-container-title:Middle East Fertility Society Journal

Author:

Al-Alfy M.E.,El-Noury M.A.,Azmy O.M.,Bebars M.A.,Alsharnoubi G.,Dawood R.M.,Nagy O.A.,Ibrahim A.K.

Publisher

Springer Science and Business Media LLC

Subject

Obstetrics and Gynecology,Reproductive Medicine

Reference22 articles.

1. Uses of cell free fetal DNA in maternal circulation;Hill;Best Pract. Res.: Clin. Obstet. Gynaecol.,2012

2. The use of cell-free fetal nucleic acids in maternal blood for non-invasive prenatal diagnosis;Wright;Human Reprod. Update,2009

3. Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis;Lo;Am. J. Hum. Genet.,1998

4. Kinetics of SRY gene appearance in maternal serum: detection by real time PCR in early pregnancy after assisted reproductive technique;Guibert;Hum. Reprod.,2003

5. Reliability of fetal sex determination using maternal plasma;Scheffer;Obstet. Gynecol.,2010

Cited by 1 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. An approach for state differentiation in nucleic acid circuits: Application to diagnostic DNA computing;Analytica Chimica Acta;2024-03

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