Fig. 3From: A 29 Mainland Chinese cohort of patients with Phelan–McDermid syndrome: genotype–phenotype correlations and the role of SHANK3 haploinsufficiency in the important phenotypesRepresentative images of patients with PMS showing mild dysmorphism. There was no significant difference between patients with 22q13 deletions encompassing more than SHANK3 gene and patients with loss of SHANK3 alone in dysmorphic featuresBack to article page