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Establishing a genomic reference for Australian Aboriginal populations
Delayed development of antibodies to S. pneumoniae in infancy is associated with the development of atopy and asthma.
Rett syndrome is a pervasive neurological disorder with impaired gait as one criterion.
A body mass index (BMI) >22kg/m2 is a risk factor for type 2 diabetes (T2D) in Aboriginal Australians.
Australia, Canada, and New Zealand are all developed nations that are home to Indigenous populations which have historically faced poorer outcomes than their...
High consumption of refined carbohydrate, in particular sugar, has been identified as a possible contributory factor in greater risk of excess weight gain.
Our case demonstrates that AML therapy, without HSCT, can be sufficient to treat this rare disease in children.
Human genetic research promises to deliver a range of health benefits to the population. Here we consider how the different levels of Indigenous research...
Multiplex ligation-dependent Probe Amplification (MLPA) has become available for the detection of a large deletion on the MECP2 gene.
In the 1990s pneumonia hospitalisation rates in Western Australia (WA) were 13 times higher in Indigenous children than in non-Indigenous children...