Mutations in CUL7, OBSL1 and CCDC8 in 3-M syndrome lead to disordered growth factor signalling.

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• Defining the phenotype of severe growth disorders, discovering new genes that control human growth and enhancing clinical practice

  Clayton, P. (Participant), Black, G. (Participant), Read, A. (Participant), Manson, F. (Participant), Hanson, D. (Participant) & Patel, L. (Participant)

  Impact: Health impacts