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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 TypeValue
Type of ResearchStrategic Basic Research
Research DivisionBiomedical and Clinical Sciences
Research GroupOphthalmology and optometry
Research FieldOphthalmology
Research Objective DivisionHealth
Research Objective GroupClinical health
Research Objective FieldClinical health not elsewhere classified
Visit Item on eCitehttp://ecite.utas.edu.au/91368
Digital Object Identifierdoi:10.1186/1471-2350-11-165
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Number of Times Cited4
Number of Downloads319