You are seeing this message because your Web browser does not support basic Web standards. Find out more about why this message is appearing and what you can do to make your experience on this site better.


ABOUT JAMA
Advanced Search

Welcome   | My Account | E-mail Alerts | Access Rights | Sign In


  Vol. 292 No. 23, December 15, 2004 TABLE OF CONTENTS
  JAMA
  •  Online Features
  Letters
 This Article
 •Full text
 •PDF
 •Send to a friend
 • Save in My Folder
 •Save to citation manager
 •Permissions
 Citing Articles
 •Citing articles on HighWire
 •Citing articles on Web of Science (3)
 •Contact me when this article is cited
 Related Content
 •Related articles
 •Similar articles in JAMA
 Topic Collections
 •Genetics
 •Genetic Counseling/ Testing/ Therapy
 •Alert me on articles by topic
 Social Bookmarking
  Add to CiteULike Add to Connotea Add to Del.icio.us Add to Digg Add to Reddit Add to Technorati Add to Twitter What's this?

Free Fetal DNA in Maternal Circulation

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

To the Editor: In reading the study by Dr Dhallan and colleagues1 regarding the percentage of fetal DNA recovered from the maternal circulation following formaldehyde treatment, we were concerned that a serial dilution method was used for estimating the fractional concentrations of fetal DNA in maternal plasma, since previous publications in this field have used real-time quantitative polymerase chain reaction (PCR) for this purpose.2-3 One would expect the serial dilution method to be less accurate and less precise than the real-time PCR method. For a given sample that is serially diluted, a test aliquot from the most diluted tube at the end of the series may be positive in one experiment and negative in another, with a frequency described by the Poisson distribution. This would result in a wider confidence interval for the measured fractional concentration of fetal DNA in maternal plasma than would real-time PCR, decreasing the precision . . . [Full Text of this Article]

Y. M. Dennis Lo, DM
loym@cuhk.edu.hk

Rossa W. K. Chiu, FRCPA; K. C. Allen Chan, MRCP; Grace T. Y. Chung, PhD
Department of Chemical Pathology
Chinese University of Hong Kong
Prince of Wales Hospital
Shatin, New Territories
Hong Kong Special Administrative Region, China



Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us   Add to Digg Digg   Add to Reddit Reddit   Add to Technorati Technorati   Add to Twitter Twitter     What's this?

RELATED ARTICLES

Free Fetal DNA in Maternal Circulation—Reply
Ravinder Dhallan, Michael Cronin, Sarah Emche, Philip Bayliss, and Marian Damewood
JAMA. 2004;292(23):2835-2836.
EXTRACT | FULL TEXT  

Methods to Increase the Percentage of Free Fetal DNA Recovered From the Maternal Circulation
Ravinder Dhallan, Wei-Chun Au, Subhendra Mattagajasingh, Sarah Emche, Philip Bayliss, Marian Damewood, Michael Cronin, Victoria Chou, and Michelle Mohr
JAMA. 2004;291(9):1114-1119.
ABSTRACT | FULL TEXT  


THIS ARTICLE HAS BEEN CITED BY OTHER ARTICLES

Microfluidics Digital PCR Reveals a Higher than Expected Fraction of Fetal DNA in Maternal Plasma
Lun et al.
Clin. Chem. 2008;54:1664-1672.
ABSTRACT | FULL TEXT  





HOME | CURRENT ISSUE | PAST ISSUES | TOPIC COLLECTIONS | CME | SUBMIT | SUBSCRIBE | HELP
CONDITIONS OF USE | PRIVACY POLICY | CONTACT US | SITE MAP
 
© 2004 American Medical Association. All Rights Reserved.