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Search Results for: Hereditary Genetics
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Environmental, personal and genetic determinants of response to vitamin D supplementation in older adults
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
Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population
Clinical and non-targeted metabolomic profiling of homozygous carriers of Transcription Factor 7-like 2 variant rs7903146
Combination of hearing screening and genetic screening for deafness-susceptibility genes in newborns
Combining TNFSF15 and ASCA IgA can be used as a predictor for the stenosis/perforating phenotype of Crohn’s disease
Common Genetic Variation in the Human CTF1 Locus, Encoding Cardiotrophin-1, Determines Insulin Sensitivity
Common variants in PERK, JNK, BIP and XBP1 genes are associated with the risk of prediabetes or diabetes-related phenotypes in a Chinese population
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