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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...
Autores principales: | Hacıhamdioğlu, Bülent, Hacıhamdioğlu, Duygu, Delil, Kenan |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2015
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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 |
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