Targeted next-generation sequencing identifies the disruption of the SHANK3 and RYR2 genes in a patient carrying a de novo t(1;22)(q43;q13.3) associated with signs of Phelan-McDermid syndrome

Overview of attention for article published in Molecular Cytogenetics, June 2020

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Targeted Next-Generation Sequencing Identifies the Disruption of the SHANK3 and RYR2 Genes in a Patient Carrying a … https://t.co/ixGvZ4NWuf

04 Jul 2020

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Targeted next-generation sequencing identifies the disruption of the SHANK3 and RYR2 genes in a patient carrying a de novo t(1;22)(q43;q13.3) associated with signs of Phelan-McDermid syndrome. https://t.co/8E8A9K7eN3 #PubMed #Autism

17 Jun 2020

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