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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Bibliografiset tiedot
Päätekijät: Jobling, Mark A., Lo, Iek Chi C., Turner, Daniel J., Bowden, Georgina R., Lee, Andrew C., Xue, Yali, Carvalho-Silva, Denise, Hurles, Matthew E., Adams, Susan M., Chang, Yuet Meng, Kraaijenbrink, Thirsa, Henke, Jürgen, Guanti, Ginevra, McKeown, Brian, van Oorschot, Roland A.H., Mitchell, R. John, de Knijff, Peter, Tyler-Smith, Chris, Parkin, Emma J.
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: 2006
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Article
Linkit: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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