The 15q11.2 BP1-BP2 Microdeletion (Burnside–Butler) Syndrome: In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental Disorders – Vide Leaf

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The 15q11.2 BP1-BP2 Microdeletion (Burnside–Butler) Syndrome In Silico Analyses of the Four Coding Genes Reveal Functional Associations with Neurodevelopmental DisordersDownload

The-15q11.2-BP1-BP2-Microdeletion-Burnside–Butler-Syndrome-In-Silico-Analyses-of-the-Four-Coding-Genes-Reveal-Functional-Associations-with-Neurodevelopmental-Disorders