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Partial duplication of the APBA2 gene in chromosome 15q13 corresponds to duplicon structures
BACKGROUND: Chromosomal abnormalities affecting human chromosome 15q11-q13 underlie multiple genomic disorders caused by deletion, duplication and triplication of intervals in this region. These events are mediated by highly homologous segments of DNA, or duplicons, that facilitate mispairing and un...
| Autores principales: | , , , , |
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| Formato: | Texto |
| Lenguaje: | English |
| Publicado: |
BioMed Central
2003
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| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC156605/ https://www.ncbi.nlm.nih.gov/pubmed/12720574 http://dx.doi.org/10.1186/1471-2164-4-15 |