Orphanet: Diagnostic du syndrome de Joubert g�nes AHI1, ARL13B, B9D1, CEP104, CEP120, CEP290, CSPP1, KIAA0556, KIAA0586, MKS1, NPHP1, PDE6D, RPGRIP1L, TCTN2, TCTN3, TMEM138, TMEM216, TMEM231, TMEM237, INPP5E, TMEM67, CC2D2A, C5ORF42, CEP41, OFD1 and TCTN1
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Diagnosis of Joubert syndrome (AHI1, ARL13B, B9D1, CEP104, CEP120, CEP290, CSPP1, KIAA0556, KIAA0586, MKS1, NPHP1, PDE6D, RPGRIP1L, TCTN2, TCTN3, TMEM138, TMEM216, TMEM231, TMEM237, INPP5E, TMEM67, CC2D2A, C5ORF42, CEP41, OFD1 and TCTN1 genes)

  • Service d'Histologie - Embryologie - Cytogntique
  • Hpital Necker-Enfants Malades
  • 149 rue de Svres
  • 75743 PARIS
  • FRANCE
  • Director of laboratory : Pr Serge ROMANA
  • More information
  • Phone : 33 (0)1 44 49 49 82
  • Additional Phone : 33 (0)1 44 49 49 83
  • Fax : 33 (0)1 44 49 04 17
  • Website
Last update: February 2020

Responsible of diagnostic test

Purpose(s)

Post-natal diagnosis

Technical procedure(s)

Molecular genetics
Sequence analysis: entire coding region
NGS sequencing (except WES)
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