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Prevalence of SMN1 deletion and duplication in carrier and normal populations: implication for genetic counselling
  1. Correspondence to:
 Dr V Cusin, Laboratoire de Biochimie Génétique, Hôpital R Debré, 48 Boulevard Sérurier, 75019 Paris, France; 
 veronica.cusin{at}wanadoo.fr
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Citation

Cusin V, Clermont O, Gérard B, et al
Prevalence of SMN1 deletion and duplication in carrier and normal populations: implication for genetic counselling

Publication history

  • First published April 1, 2003.
Online issue publication 
April 27, 2016

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