We’ve been asked by our friends at the University of Sheffield to share details of a new research project, looking at communication abilities in children with rare genetic conditions.
They are interested in families who have a child aged between 2 years and 15 years 11 months old with a gene change or chromosome deletion involving the following:
SYNGAP1 gene change or 6p21 deletion
DYRK1A gene change or 21q22 deletion
ANKRD11 gene change or 16q24 deletion
ARID1B gene change or 6q25 deletion
MED13L gene change or 12q24 deletion
SETD5 gene change or 3p25 deletion
ADNP gene change or 20q13 deletion
TRIP12 gene change or 2q26 deletion
Please see details below or click here to visit their website to find out more.