Identification of Two PAX3 MutationsCausing Waardenburg Syndrome, one Within the Paired Domain (M62V) and the Other Downstream of the Homeodomain (Q282X)

Find Full text
Publication year
1998
Author(s)
Hol, F.A.
Geurds, M.P.A.
Cremers, C.W.R.J.
Hamel, B.C.J.
Mariman, E.C.M.
Number of pages
3 p.
Source
Human Mutation, S1, (1998), pp. S145-S147
ISSN
Publication type
Article / Letter to editor
Please use this identifier to cite or link to this item: https://hdl.handle.net/2066/166809   https://hdl.handle.net/2066/166809
Display more details

Upload full text

Use your RU credentials (u/z-number and password) to log in with SURFconext to upload a file for processing by the repository team.