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    Sequencing of a patient with balanced chromosome abnormalities and neurodevelopmental disease identifies disruption of multiple high risk loci by structural variation by Blake, Jonathon (Author) , Riddell, Andrew (Author) , Theiß, Susanne (Author) , Gonzalez, Alexis Perez (Author) , Haase, Bettina (Author) , Jauch, Anna (Author) , Janssen, Johannes W. G. (Author) , Ibberson, David (Author) , Pavlinic, Dinko (Author) , Moog, Ute (Author) , Benes, Vladimir (Author) , Runz, Heiko (Author) ,


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