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...
Αποθηκεύτηκε σε:
| Εκδόθηκε σε: | BMC Genomics |
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| Κύριοι συγγραφείς: | , , , , |
| Μορφή: | Artigo |
| Γλώσσα: | Inglês |
| Έκδοση: |
BMC
2003
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| Θέματα: | |
| Διαθέσιμο Online: | 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 |
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