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Detection of Copy Number Variation (CNV) by SNP-Allelotyping
Determinants Of Oral corticosteroid Responsiveness in Wheezing Asthmatic Youth (DOORWAY
Clinical and non-targeted metabolomic profiling of homozygous carriers of Transcription Factor 7-like 2 variant rs7903146
Differential Methylation of TCF7L2 Promoter in Peripheral Blood DNA in Newly Diagnosed, Drug-NaÃ¯ve Patients with Type 2 Diabetes
Combination of hearing screening and genetic screening for deafness-susceptibility genes in newborns
Digital Genotyping of Macrosatellites and Multicopy Genes Reveals Novel Biological Functions Associated with Copy Number Variation of Large Tandem Repeats
Combining TNFSF15 and ASCA IgA can be used as a predictor for the stenosis/perforating phenotype of Crohn’s disease
Direct Evidence on the Contribution of a Missense Mutation in GDF9 to Variation in Ovulation Rate of Finnsheep
Common Genetic Variation in the Human CTF1 Locus, Encoding Cardiotrophin-1, Determines Insulin Sensitivity
Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population