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  Genetic causes of Neurodevelopmental Delay in Children: translation and interpretation of novel pathogenic copy number variants and novel rare exonic mutations into clinical genetic practice

  Curran, S. (Primary Investigator), Bolton, P. (Co-Investigator), Collier, D. (Co-Investigator), Dobson, R. (Co-Investigator), Furney, S. (Co-Investigator) & Pal, D. (Co-Investigator)

  NIHR National Institute For Health & Care Research

  1/10/2010 → 30/09/2011

  Project: Research

• Genetic causes of Neurodevelopmental Delay in Children: translation and interpretation of novel pathogenic copy number variants and novel rare exonic mutations into clinical genetic practice

  Curran, S. (Primary Investigator), Bolton, P. (Co-Investigator), Collier, D. (Co-Investigator), Dobson, R. (Co-Investigator), Furney, S. (Co-Investigator) & Pal, D. (Co-Investigator)

  NIHR National Institute For Health & Care Research

  1/04/2010 → 31/03/2011

  Project: Research