Publication New pathogenic thyrtropin receptor mutations decipher differentiated activity switching at a conserved helix 6 motif of family A GPCR
Publication Neonatal white matter abnormality predicts childhood motor impairment in very preterm children
Publication Integrated genomic analysis of relapsed childhood acute lymphoblastic leukemia reveals therapeutic strategies
Publication Hospitalisation with infection, asthma and allergy in Kawasaki disease patients and their families: genealogical analysis using linked population data.
