Latest Physician Education Resources
Mutations in the spliceosome machinery, a novel and ubiquitous pathway in leukemogenesis
Autosomal recessive Emery-Dreifuss muscular dystrophy caused by a novel mutation (R225Q) in the lamin A/C gene identified by exome sequencing
Base-Resolution Analysis of 5-Hydroxymethylcytosine in the Mammalian Genome
A Low-Cost Exon Capture Method Suitable for Large-Scale Screening of Genetic Deafness by the Massively-Parallel Sequencing Approach
Applications of targeted gene capture and next-generation sequencing technologies in studies of human deafness and other genetic disabilities
Nature Readers Flirt With Personal Genomics
Transcriptional profiling reveals gland-specific differential expression in the three major salivary glands of the adult mouse
Epigenetic alterations in TRAMP mice: epigenome DNA methylation profiling using MeDIP-seq
A novel missense mutation in GIPC3 causes sensorineural hearing loss in an Iranian family revealed by targeted next-generation sequencing
Tread carefully: A functional variant in the human NADPH oxidase 4 (NOX4) is not disease causing
