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High rates of de novo 15q11q13 inversions in human spermatozoa
Low-Copy Repeats predispose the 15q11-q13 region to non-allelic homologous recombination. We have already demonstrated that a significant percentage of Prader-Willi syndrome (PWS) fathers have an increased susceptibility to generate 15q11q13 deletions in spermatozoa, suggesting the participation of...
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| Main Authors: | , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BioMed Central
2012
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3293048/ https://ncbi.nlm.nih.gov/pubmed/22309495 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1755-8166-5-11 |
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