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Detection of Copy Number Variation (CNV) by SNP-Allelotyping
Determinants Of Oral corticosteroid Responsiveness in Wheezing Asthmatic Youth (DOORWAY
Digital Genotyping of Macrosatellites and Multicopy Genes Reveals Novel Biological Functions Associated with Copy Number Variation of Large Tandem Repeats
CCDC26 Gene Polymorphism and Glioblastoma Risk in the Han Chinese Population
CFI-rs7356506 is a genetic protective factor for acute anterior uveitis in Chinese patients
Characterisation of Genetic Variation in ST8SIA2 and Its Interaction Region in NCAM1 in Patients with Bipolar Disorder
CHD7 Deficiency in â€œLooperâ€, a New Mouse Model of CHARGE Syndrome, Results in Ossicle Malformation, Otosclerosis and Hearing Impairment
Circulating IGF1 and IGF2 and SNP genotypes in pregnant and non-pregnant women and men
Blood cis-eQTL Analysis Fails to Identify Novel Association Signals among Sub-Threshold Candidates from Genome-Wide Association Studies in Restless Legs Syndrome
Bone Morphogenetic Protein 6 Polymorphisms Are Associated with Radiographic Progression in Ankylosing Spondylitis