Seminars in Fetal & Neonatal Medicine
Volume 13, Issue 2 , Pages 76-83, April 2008

Non-invasive prenatal diagnosis of single gene disorders: How close are we?

  • Gail Norbury

      Affiliations

    • NE Thames Regional Molecular Genetics Laboratory, Camelia Botnar Laboratories, Great Ormond Street Hospital, Great Ormond Street, London WC1N 3JH, UK
    • Corresponding Author InformationCorresponding author. Tel.: +44 207 905 2659; fax: +44 207 813 8196.
    • ,
  • Chris J. Norbury

      Affiliations

    • Sir William Dunn School of Pathology, University of Oxford, Oxford, UK

published online 31 January 2008.

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.

PII: S1744-165X(07)00154-0

doi:10.1016/j.siny.2007.12.008

Seminars in Fetal & Neonatal Medicine
Volume 13, Issue 2 , Pages 76-83, April 2008

Article Tools

* Image Usage & Resolution