C21ORF105, A chromosome 21-encoded mRNA, is not a discriminative marker gene for prediction of Down syndrome in maternal plasma-Reference-Cited by-同舟云学术

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C21ORF105, A chromosome 21-encoded mRNA, is not a discriminative marker gene for prediction of Down syndrome in maternal plasma

Published:2007 Issue:2 Volume:27 Page:146-149
ISSN:0197-3851
Container-title:Prenatal Diagnosis
language:en
Short-container-title:Prenat. Diagn.

Author:

Go A. T. J. I.,Visser A.,Mulders M. A. M.,Twisk J. W. R.,Blankenstein M. A.,van Vugt J. M. G.,Oudejans C. B. M.

Publisher

Wiley

Subject

Genetics (clinical),Obstetrics and Gynecology

Reference6 articles.

1. Detection of Placental Transcription Factor mRNA in Maternal Plasma

2. Gene expression profile of trisomy 21 placentas: A potential approach for designing noninvasive techniques of prenatal diagnosis

3. mRNA of placental origin is readily detectable in maternal plasma

4. The Concentration of Circulating Corticotropin-releasing Hormone mRNA in Maternal Plasma Is Increased in Preeclampsia

5. Detection of Chromosome 21-encoded mRNA of Placental Origin in Maternal Plasma

Cited by 10 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. The Role of RNAs and microRNAs in Non-Invasive Prenatal Diagnosis;Journal of Clinical Medicine;2014-05-06

2. Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012;Human Reproduction Update;2013-02-08

3. Validity of Different Methods to Prenatal Screening for Down's Syndrom During First and Second Trimester Pregnancy of Chinese Women;BIOMED ENVIRON SCI;2013

4. Tracking fetal development through molecular analysis of maternal biofluids;Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease;2012-12

5. Second Trimester Prenatal Screening for Down’s Syndrome in Mainland Chinese Subjects using Double-Marker Analysis of α-fetoprotein and β-human Chorionic Gonadotropin Combined with Measurement of Nuchal Fold Thickness;Annals of the Academy of Medicine, Singapore;2011-07-15

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