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...

Descripció completa

Dades bibliogràfiques

Publicat a:	BMC Genomics
Autors principals:	Sutcliffe, James S, Han, Michael K, Amin, Taneem, Kesterson, Robert A, Nurmi, Erika L
Format:	Artigo
Idioma:	Inglês
Publicat:	BMC 2003
Matèries:	Research Article
Accés en línia:	https://ncbi.nlm.nih.govhttps://pmc.ncbi.nlm.nih.gov/articles/PMC156605/ https://ncbi.nlm.nih.govhttps://pubmed.ncbi.nlm.nih.gov/12720574/ https://ncbi.nlm.nih.govhttps://doi.org/10.1186/1471-2164-4-15
Etiquetes:	Afegir etiqueta Sense etiquetes, Sigues el primer a etiquetar aquest registre!