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

Syed K Rafi, Merlin G Butler
2020 Prime Archives in Molecular Sciences  
doi:10.37247/pamolscs.1.2020.17 fatcat:ufqxnqmfkvfrtckjr7ggykpg3a