Associated Papers
3-M syndrome: evolution of the phenotype over time.
Bacchi I et al.
Italian Journal of Pediatrics, 2025
41437277 (PubMed )
Supplement: 13052_2025_2172_MOESM1_ESM.xlsx › S3_CCDC8
3-M syndrome: a growth disorder associated with IGF2 silencing.
Murray PG et al.
Endocrine Connections, 2013
Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling.
Hanson D et al.
Journal of Molecular Endocrinology, 2012
Exome sequencing identifies CCDC8 mutations in 3-M syndrome, suggesting that CCDC8 contributes in a pathway with CUL7 and OBSL1 to control human growth.
Hanson D et al.
American Journal of Human Genetics, 2011
The genetics of 3-M syndrome: unravelling a potential new regulatory growth pathway.
Hanson D et al.
Hormone Research in Paediatrics, 2011
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