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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Detalles Bibliográficos
Autores principales: Baldwin, Isaac, Shafer, Robin L., Hossain, Waheeda A., Gunewardena, Sumedha, Veatch, Olivia J., Mosconi, Matthew W., Butler, Merlin G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7914695/
https://www.ncbi.nlm.nih.gov/pubmed/33562221
http://dx.doi.org/10.3390/ijms22041660

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7914695/
https://www.ncbi.nlm.nih.gov/pubmed/33562221
http://dx.doi.org/10.3390/ijms22041660

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