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Wellcome Trust Centre for Human Genetics, University of Oxford | 論文
- Family-based analysis of vitamin D receptor gene polymorphisms and type 1 diabetes in the population of South Croatia
- A genome-wide scan in forty large pedigrees with multiple sclerosis
- Identification of two HEXA mutations causing infantile-onset Tay-Sachs disease in the Persian population
- A genome-wide scan of male sexual orientation
- Parent-of-origin of HLA-DRB1^*1501 and age of onset of multiple sclerosis