x

Search for a research project

* (*) mandatory field

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

    • Type of research project :
      • Diagnostic tool/protocol development
      • Human physiopathology study
      • Mutations search
  • Website
  • Funded by an IRDiRC member
    • Funding body(ies) :
      • INSTITUTO DE SALUD CARLOS III (ISCIII)

Download more information on this project

  • 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
  • SPAIN
  • More information
  • Phone  : 34 94 600 6532
  • Fax  : -
  • Website
Last update: January 2018

Additional information

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.