Adelaide Research & Scholarship
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https://hdl.handle.net/2440/116371
| Type: | Theses |
| Title: | Investigation of the role of the MID1 and MID2 genes in the Opitz syndrome |
| Author: | Allen, Lillian Rose |
| Issue Date: | 2003 |
| School/Discipline: | School of Molecular and Biomedical Sciences |
| Abstract: | To determine whether or not the MID1 and MID2 genes contribute to the Optiz Syndrome (OS) phenotype, a mutation screen was undertaken. Fifteen Australasian and one British patient diagnosed as having Optiz Syndrome were screened for mutations in the MID1 and MID2 genes. The zebrafish (Danio rerio) was used as a model system in which to find a MID1 homologue in order to further analyse the function of MID1 and how it may cause the OS phenotype. |
| Dissertation Note: | Thesis (M.Sc.) -- University of Adelaide, School of Molecular and Biomedical Sciences, 2003 |
| Keywords: | Sex Chromosome Abnormalities -- familial & genetic |
| Description: | NOTE: Pages 57, 65, 178 & 186 are missing from the print and digital copies of the thesis |
| Provenance: | This electronic version is made publicly available by the University of Adelaide in accordance with its open access policy for student theses. Copyright in this thesis remains with the author. This thesis may incorporate third party material which has been used by the author pursuant to Fair Dealing exceptions. If you are the owner of any included third party copyright material you wish to be removed from this electronic version, please complete the take down form located at: http://www.adelaide.edu.au/legals |
| Appears in Collections: | Research Theses |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| 01front.pdf | 538.16 kB | Adobe PDF | View/Open | |
| 02whole.pdf | 12.2 MB | Adobe PDF | View/Open |
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