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The 15q11.2 BP1–BP2 Microdeletion Syndrome: A Review

Patients with the 15q11.2 BP1–BP2 microdeletion can present with developmental and language delay, neurobehavioral disturbances and psychiatric problems. Autism, seizures, schizophrenia and mild dysmorphic features are less commonly seen. The 15q11.2 BP1–BP2 microdeletion involving four genes (i.e.,...

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Bibliografski detalji
Izdano u:Int J Mol Sci
Glavni autori: Cox, Devin M., Butler, Merlin G.
Format: Artigo
Jezik:Inglês
Izdano: MDPI 2015
Teme:
Online pristup:https://ncbi.nlm.nih.gov/pmc/articles/PMC4346944/
https://ncbi.nlm.nih.gov/pubmed/25689425
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3390/ijms16024068
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