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Polymorphic Variation in Human Meiotic Recombination
In this study, our phenotype of interest is meiotic recombination. Using genotypes of ∼6,000 SNP markers in members of the Centre d'Étude du Polymorphisme Humain Utah pedigrees, we found extensive individual variation in the number of female and male recombination events. The locations and freq...
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| Huvudupphovsmän: | , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
The American Society of Human Genetics
2007
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1821106/ https://ncbi.nlm.nih.gov/pubmed/17273974 |
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