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Identify Candidate Causal SNPs and Pathway
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Genetics of atrial fibrillation: rare mutations, common variants and clinical relevance?].
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Influence of WNT4 VEZT FSHB and SIRT1 SNPs in Endometriosis: a Case Control Study of the Sardinian P…
The Drug Induced Renal Injury Consortium
Investigating the Genetic Basis of Pseudoexfoliation Syndrome and Angle-closure Glaucoma
Pharmacogenomic Association Study in Indian Children With Acute Lymphoblastic Leukemia
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