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New blood test to boost diagnosis for rare genetic diseases in kids

The simple blood test, developed by researchers from the University of Melbourne and Murdoch Children's Research Institute (MCRI), eliminates the need for costly and invasive procedures

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Image for representational purpose only. Photo Courtesy: istock

Image for representational purpose only. Photo Courtesy: istock

Australian researchers have developed a new blood test that can rapidly diagnose rare genetic diseases in babies and children.  

The simple blood test, developed by researchers from the University of Melbourne and Murdoch Children's Research Institute (MCRI), eliminates the need for costly and invasive procedures.

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