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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
Defining the Contribution of CNTNAP2 to Autism Susceptibility
Defining the disease liability of variants in the cystic fibrosis transmembrane conductance regulator gene
Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing
Differential Expression of the Tumor Suppressor A-Kinase Anchor Protein 12 in Human Diffuse and Pilocytic Astrocytomas Is Regulated by Promoter Methylation
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