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...

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Detalles Bibliográficos
Autores principales: Sutcliffe, James S, Han, Michael K, Amin, Taneem, Kesterson, Robert A, Nurmi, Erika L
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Research Article
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

Internet

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

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