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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:
F2RL3 Methylation as a Biomarker of Current and Lifetime Smoking Exposures
Effect of Variation of ABCB1 and ABCC3 Genotypes on the Survival of Bone Tumor Cases after Chemotherapy
Family environment and adult resilience: contributions of positive parenting and the oxytocin receptor gene
Effects of polymorphisms in nucleotide excision repair genes on glioma risk in a Chinese population