G73809[Secondary Source ID] - Search Results

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Are sequence family variants useful for identifying deletions in the human Y chromosome?

Repping S, Korver CM, Oates RD, Silber S, van der Veen F, Page DC, Rozen S. Repping S, et al. Am J Hum Genet. 2004 Sep;75(3):514-7; author reply 517-9. doi: 10.1086/423394. Am J Hum Genet. 2004. PMID: 15284951 Free PMC article. No abstract available.

Polymorphism for a 1.6-Mb deletion of the human Y chromosome persists through balance between recurrent mutation and haploid selection.

Repping S, Skaletsky H, Brown L, van Daalen SK, Korver CM, Pyntikova T, Kuroda-Kawaguchi T, de Vries JW, Oates RD, Silber S, van der Veen F, Page DC, Rozen S. Repping S, et al. Nat Genet. 2003 Nov;35(3):247-51. doi: 10.1038/ng1250. Epub 2003 Oct 5. Nat Genet. 2003. PMID: 14528305

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