Skip to main content
. 2023 Apr 14;31(8):859–868. doi: 10.1038/s41431-023-01359-z

Table 1.

Frequency of features in individuals with a clinical and genetic diagnosis of Meier-Gorlin syndrome.

graphic file with name 41431_2023_1359_Tab1_HTML.gif

Information was derived from the reported cases in the literature and clinical information provided, so the number of cases in the literature likely underestimates the true number of affected individuals, especially for established disease genes. na information not available. IUGR intra-uterine growth retardation, ID intellectual disability, DD developmental delay.