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Failure to recombine is a common feature of human oogenesis
Failure of homologous chromosomes to recombine is arguably the most important cause of human meiotic nondisjunction, having been linked to numerous autosomal and sex chromosome trisomies of maternal origin. However, almost all information on these “exchangeless” homologs has come from genetic mappin...
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| Publicado no: | Am J Hum Genet |
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| Main Authors: | , , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2021
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7820622/ https://ncbi.nlm.nih.gov/pubmed/33306948 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.ajhg.2020.11.010 |
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