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Christine Petit

Unité de Génétique des Déficits Sensoriels


Institute Pasteur

25 rue du Dr. Roux



Name/email consistency: high



  • Unité de Génétique des Déficits Sensoriels, CNRS URA 1968, Institute Pasteur, 25 rue du Dr. Roux, France. 1999 - 2006
  • Unité de Génétique Moléculaire Humaine, URA 1968, CNRS, Institut Pasteur, Paris, France. 1996 - 2004


  1. From deafness genes to hearing mechanisms: harmony and counterpoint. Petit, C. Trends. Mol. Med (2006) [Pubmed]
  2. Memorial lecture-hereditary sensory defects: from genes to pathogenesis. Petit, C. Am. J. Med. Genet. A (2004) [Pubmed]
  3. Molecular genetics of hearing loss. Petit, C., Levilliers, J., Hardelin, J.P. Annu. Rev. Genet. (2001) [Pubmed]
  4. Usher syndrome: from genetics to pathogenesis. Petit, C. Annu. Rev. Genomics. Hum. Genet (2001) [Pubmed]
  5. The zebrafish eya1 gene and its expression pattern during embryogenesis. Sahly, I., Andermann, P., Petit, C. Dev. Genes Evol. (1999) [Pubmed]
  6. Genes responsible for human hereditary deafness: symphony of a thousand. Petit, C. Nat. Genet. (1996) [Pubmed]
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