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A putative human infertility allele of the meiotic recombinase DMC1 does not affect fertility in mice
Whole-exome or whole-genome sequencing is becoming routine in clinical situations for identifying mutations underlying presumed genetic causes of disease including infertility. While this is a powerful approach for implicating polymorphisms or de novo mutations in genes plausibly related to the phen...
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| Publicado no: | Hum Mol Genet |
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| Main Authors: | , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Oxford University Press
2018
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6216207/ https://ncbi.nlm.nih.gov/pubmed/30085085 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddy286 |
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