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  • Evaluating the association between keratoconus and the corneal thickness genes in an independent Australian Population
  • Exome Sequencing and Linkage Analysis Identified Tenascin-C (TNC) as a Novel Causative Gene in Nonsyndromic Hearing Loss
  • Exome sequencing reveals HINT1 mutations as a cause of distal hereditary motor neuropathy
  • Expression and DNA methylation status of microRNA-375 in patients with type 2 diabetes mellitus
  • Expression and Methylation of FGF2, TGF-? and Their Downstream Mediators during Different Developmental Stages of Leg Muscles in Chicken
  • Expression and mutational status of treatment-relevant targets and key oncogenes in 123 malignant salivary gland tumours:
  • Deep Resequencing of GWAS Loci Identifies Rare Variants in CARD9, IL23R and RNF186 That Are Associated with Ulcerative Colitis
  • Effect of NR3C2 genetic polymorphisms on the blood pressure response to enalapril treatment
  • Defining the Contribution of CNTNAP2 to Autism Susceptibility
  • Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene
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