Fig. 4
From: Molecular and phenotypic characteristics of Bardet-Biedl syndrome in Chinese patients
Genotype–phenotype correlations in our cohort of BBS patients. A Distribution of primary and secondary features between patients with mutations in BBSome genes and chaperonin-like genes. B The age of onset and diagnosis of patients with mutations in BBS2,7,9 versus BBS10,12. Distribution of primary and secondary features between patients with mutations in BBSome genes and chaperonin-like genes. C BMI, visual score, and syndromic score in BBS patients with BBS2,7,9 mutations and BBS10,12 mutations. *p < 0 .05, **p < 0 .01