rss

Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype

Author Correction

Please note that there is an error in the reverse primer sequence used for amplification of the intragenic microsatellite polymorphic marker of the SIM1 gene.
The correct sequence is shown here:

5'-CTCTCCTGCCTGCTGATC-3'

    About the toc

    1. doi: 10.1136/jmg.39.8.594 J Med Genet 1 August 2002 vol. 39 no. 8 594-596
    1. Extract
    2. Full text
    3. PDF
    4. Author Correction

    Register for free content

    The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.

    Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.