Hendry, M. (2003) Parietal foramina with cleidocranial dysplasia is caused by mutation in MSX2. European Journal of Human Genetics, 11(11), pp. 892-895.
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| Item Type: | Articles |
|---|---|
| Status: | Published |
| Refereed: | Yes |
| Glasgow Author(s) Enlighten ID: | Hendry, Professor Martin |
| Authors: | Hendry, M. |
| College/School: | College of Science and Engineering > School of Physics and Astronomy |
| Journal Name: | European Journal of Human Genetics |
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