Missingness in the T1DGC MHC fine-mapping SNP data: association with HLA genotype and potential influence on genetic association studies
Author:
Publisher
Wiley
Subject
Endocrinology,Endocrinology, Diabetes and Metabolism,Internal Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1463-1326.2008.01010.x/fullpdf
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3. A high-resolution survey of deletion polymorphism in the human genome;Conrad;Nat Genet,2006
4. Copy number variants and common disorders: filling the gaps and exploring complexity in genome-wide association studies;Estivill;PLOS Genet,2007
5. In polymorphic genomic regions indels cluster with nucleotide polymorphism: quantum genomics;Longman-Jacobsen;Gene,2003
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