Genomic, Clinical, and Behavioral Characterization of 15q11.2 BP1-BP2 Deletion (Burnside-Butler) Syndrome in Five Families

The 15q11.2 BP1-BP2 deletion (Burnside-Butler) syndrome is emerging as the most common cytogenetic finding in patients with neurodevelopmental or autism spectrum disorders (ASD) presenting for microarray genetic testing. Clinical findings in Burnside-Butler syndrome include developmental and motor d...

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Veröffentlicht in:Int J Mol Sci
Hauptverfasser: Baldwin, Isaac, Shafer, Robin L., Hossain, Waheeda A., Gunewardena, Sumedha, Veatch, Olivia J., Mosconi, Matthew W., Butler, Merlin G.
Format: Artigo
Sprache:Inglês
Veröffentlicht: MDPI 2021
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Article
Online Zugang:https://ncbi.nlm.nih.gov/pmc/articles/PMC7914695/
https://ncbi.nlm.nih.gov/pubmed/33562221
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms22041660
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