| Hattersley, K and Laurie, KJ and Liebelt, JE and Gecz, J and Durkin, SR and Craig, JE and Burdon, KP, “A novel syndrome of paediatric cataract, dysmorphism, ectodermal features, and developmental delay in Australian Aboriginal family maps to 1p35.3-p36.32”, BMC Medical Genetics, 11 (1) Article 165. ISSN 1471-2350 (2010) [Refereed Article] |
| Data Type | Value |
|---|
| Type of Research | Strategic Basic Research |
| Research Division | Biomedical and Clinical Sciences |
| Research Group | Ophthalmology and optometry |
| Research Field | Ophthalmology |
| Research Objective Division | Health |
| Research Objective Group | Clinical health |
| Research Objective Field | Clinical health not elsewhere classified |
| Visit Item on eCite | http://ecite.utas.edu.au/91368 |
| Digital Object Identifier | doi:10.1186/1471-2350-11-165 |
| Scopus Source URL | View the full record on Scopus |
| Scopus Citing URL | View the list of citing articles on Scopus |
| Web of Science® Source URL | View the full record on Web of Science® |
| Web of Science® Citing URL | View the list of citing articles on Web of Science® |
| Web of Science® Related URL | View the list of related articles on Web of Science® |
| Number of Times Cited | 4 |
| Number of Downloads | 328 |
