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22q11 deletion syndrome: current perspective

Chromosome 22q11 is characterized by the presence of chromosome-specific low-copy repeats or segmental duplications. This region of the chromosome is very unstable and susceptible to mutations. The misalignment of low-copy repeats during nonallelic homologous recombination leads to the deletion of t...

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Detalles Bibliográficos
Autores principales: Hacıhamdioğlu, Bülent, Hacıhamdioğlu, Duygu, Delil, Kenan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4445702/
https://www.ncbi.nlm.nih.gov/pubmed/26056486
http://dx.doi.org/10.2147/TACG.S82105