Browsing "Special Research Centre for the Molecular Genetics of Development (CMGD)" by Author Goodwin, B.
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Preview | Issue Date | Title | Author(s) |
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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. |