Publication | Open Access
Mutations in DVL1 Cause an Osteosclerotic Form of Robinow Syndrome
Kieran J. Bunn,
Phil Daniel,
Heleen S. Rösken,
Adam C. O’Neill,
Sophia Cameron‐Christie,
Tim Morgan,
Han G. Brunner,
Angeline Lai,
Henricus P. M. Kunst,
David Markie,
The American Journal of Human GeneticsGenetic DisorderGeneticsPathologyMedicineRobinow Syndrome