Adelaide Research & Scholarship
Browsing "Special Research Centre for the Molecular Genetics of Development (CMGD)" by Author Cox, L.
Showing results 1 to 3 of 3
Preview | Issue Date | Title | Author(s) |
| 2002 | Isolation and characterisation of the chick orthologue of the Opitz syndrome gene, Mid1, supports a conserved role in vertebrate development | Richman, J.; Fu, K.; Cox, L.; Sibbons, J.; Cox, T. |
| 2000 | New mutations in MID1 provide support for loss of function as the cause of X-linked Optiz syndrome | Cox, T.; Allen, L.; Cox, L.; Hopwood, B.; Goodwin, B.; Haan, E.; Suthers, G. |
| 2004 | The major splice variant of human 5-aminolevulinate synthase-2 contributes significantly to erythroid heme biosynthesis | Cox, T.; Sadlon, T.; Schwarz, Q.; Matthews, C.; Wise, P.; Cox, L.; Bottomley, S.; May, B. |