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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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