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Deletion of the SIM1 gene (6q16.2) in a patient with a Prader-Willi-like phenotype
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  1. Correspondence to:
 Dr M Vekemans, Département de Génétique, Hôpital Necker-Enfants Malades, 149 rue de Sévres, 75015 Paris, France;
 vekemans{at}necker.fr
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Citation

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

Publication history

  • First published August 1, 2002.
Online issue publication 
August 01, 2002
  • 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'

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