Deletion variants of RABGAP1L, 10q21.3 and C4 are associated with the risk of systemic lupus erythematosus in Korean women

De novo copy number variations in cloned dogs from the same nuclear donor

Clinical applications of next-generation sequencing in colorectal cancers

Application of array comparative genomic hybridization in chronic myeloid leukemia

Recurrent Loss of the FHIT Gene and its Impact on Lymphatic Metastasis in Early Oral Squamous Cell Carcinoma

The APOM polymorphism as a novel risk factor for dyslipidaemia in rheumatoid arthritis: a possible shared link between disease

CNVRuler: A copy number variation-based case-control association analysis tool

Stuffer-free multiplex ligation-dependent probe amplification based on conformation-sensitive capillary electrophoresis: a nove

Simultaneous copy number gains of NUPR1 and ERBB2 predicting poor prognosis in early-stage breast cancer

Precise H1N1 swine influenza detection using stuffer-free multiplex ligation-dependent probe amplification in conformation-sens

Identifying Copy Number Variants under Selection in Geographically Structured Populations Based on F-statistics

Web-based database and viewer of East asian copy number variations

Effect of Combining Multiple CNV Defining Algorithms on the Reliability of CNV Calls from SNP Genotyping Data

Common variants at the promoter region of the APOM confer a risk of rheumatoid arthritis

Strategy for high-fidelity multiplex DNA copy number assay system using capillary electrophoresis devices