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Contribution of mutations in X linked genes versus mutations in autosomes in pairs of brothers with intellectual disabilities without etiology, and no other family history. Study by Next Generation Sequencing (terminated)

    • Type of research project :
      • Diagnostic tool/protocol development
      • Human physiopathology study
      • Mutations search
  • Website
    • Funding body(ies) :

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  • Investigator of research project

  • Dr María-Isabel TEJADA
  • Grupo de Investigación en Etiología, Prevención y Tratamiento de Enfermedades Genéticas
  • Hospital Universitario Cruces - Osakidetza
  • Plaza de Cruces s/n
  • 48903 BARAKALDO
  • More information
  • Phone  : 34 94 600 6532
  • Fax  : -
  • Website
Last update: January 2019

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