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Structural variation on the short arm of the human Y chromosome: recurrent multigene deletions encompassing Amelogenin Y
Structural polymorphism is increasingly recognised as a major form of human genome variation, and is particularly prevalent on the Y chromosome. Assay of the Amelogenin Y gene (AMELY) on Yp is widely used in DNA-based sex testing, and sometimes reveals males who have interstitial deletions. In a col...
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| Main Authors: | , , , , , , , , , , , , , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2006
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2590852/ https://ncbi.nlm.nih.gov/pubmed/17189292 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddl465 |
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