P.Q. Thomas
Gene Discovery Unit
The Murdoch Children's Research Institute
Royal Children's Hospital
Flemington Road
Australia
Name/email consistency: high
- Heterozygous HESX1 mutations associated with isolated congenital pituitary hypoplasia and septo-optic dysplasia. Thomas, P.Q., Dattani, M.T., Brickman, J.M., McNay, D., Warne, G., Zacharin, M., Cameron, F., Hurst, J., Woods, K., Dunger, D., Stanhope, R., Forrest, S., Robinson, I.C., Beddington, R.S. Hum. Mol. Genet. (2001)