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</html><thumbnail_url>https://static.timesnewsgroup.com.au/prod/uploads/sites/28/2022/01/272752476_349798966964539_2124405484896874221_n-768x768-1.jpg</thumbnail_url><thumbnail_width>768</thumbnail_width><thumbnail_height>768</thumbnail_height><description>Victorian researchers from Murdoch Children&#x2019;s Research Institute &#x2013; MCRI have created a new screening test that could pave the way for earlier and easier diagnosis of three rare genetic disorders in babies. The new screening method identifies Prader Willi, Angelman and Dup15q syndromes in newborns. Developed thanks to a Victorian Government research grant, the new [...]Read More...</description></oembed>
