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  • Common TGF?2, BMP4, and FOXC1 variants are not associated with primary open-angle glaucoma
  • Application of a high-throughput genotyping method for loci exclusion in non-consanguineous Australian pedigrees with autosomal recessive retinitis pigmentosa
  • The 1200 Patients Project: Creating a New Medical Model System for Clinical Implementation of Pharmacogenomics
  • PPARA: A Novel Genetic Determinant of CYP3A4 In Vitro and In Vivo
  • Concordance of DMET Plus Genotyping Results With Those of Orthogonal Genotyping Methods
  • IL10 polymorphisms influence neonatal immune responses, atopic dermatitis, and wheeze at age 3 years
  • Association of TCF4 and CLU polymorphisms with Fuchs´endothelial dystrophy and implication of CLU and TGFBI proteins in the disease progress
  • Association of ELMO1 gene polymorphisms with diabetic nephropathy in Chinese population:
  • A large-sample assessment of possible association between ischaemic stroke and rs12188950 in the PDE4D gene
  • Genetic variant rs4982958 at 14q11.2 is associated with allergic rhinitis in a Chinese Han population
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