Skip to main content
Fig. 1 | BMC Pediatrics

Fig. 1

From: High prevalence of cardiovascular risk factors in children and adolescents with Williams-Beuren syndrome

Fig. 1

The chromosome 7q11.23 microdeletion was associated with the Williams-Beuren syndrome phenotypes in all subjects. Overall, 26 of 32 patients (82 %) showed the typical deletion responsible for Williams-Beuren syndrome (denoted as A), and 6 patients showed atypical deletions shorter than A (B, n = 2; C, n = 3; and D, n = 1)

Back to article page

BMC Pediatrics

ISSN: 1471-2431

Contact us