Genomic Disorders: Molecular Mechanisms for Rearrangements and Conveyed Phenotypes
Rearrangements of our genome can be responsible for inherited as well as sporadic traits. The analyses of chromosome breakpoints in the proximal short arm of Chromosome 17 (17p) reveal nonallelic homologous recombination (NAHR) as a major mechanism for recurrent rearrangements whereas nonhomologous...
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| Hoofdauteurs: | , |
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| Formaat: | Text |
| Taal: | Engels |
| Gepubliceerd in: |
Public Library of Science
2005
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| Onderwerpen: | |
| Online toegang: | https://pmc.ncbi.nlm.nih.gov/articles/PMC1352149/ https://pubmed.ncbi.nlm.nih.gov/16444292 http://dx.doi.org/10.1371/journal.pgen.0010049 |
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