Article Text

Download PDFPDF


Statistics from

Request Permissions

If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.

Faivre L, Cormier-Daire V, Lapierre JM, et al. Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype (J Med Genet 2002;39:594–96). An erratum has been detected in the reverse primer sequence used for amplification of the intragenic microsatellite polymorphic marker of the SIM1 gene. The sequence should read 5′-CTCTCCTGCCTGCTGATC-3′ instead of 5′-GATCAGCAGGCAGGAGAG-3′.

Linked Articles