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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Detalles Bibliográficos
Autores principales: Molina, Òscar, Anton, Ester, Vidal, Francesca, Blanco, Joan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293048/
https://www.ncbi.nlm.nih.gov/pubmed/22309495
http://dx.doi.org/10.1186/1755-8166-5-11

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293048/
https://www.ncbi.nlm.nih.gov/pubmed/22309495
http://dx.doi.org/10.1186/1755-8166-5-11

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