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Correlation Analysis of FPGS rs10760502G>A Polymorphism with Prognosis and MTX-related Toxicity in Pediatric B-cell Acute Lymphoblastic Leukemia
CREM Variants rs4934540 and rs2295415 Conferred Susceptibility to Non-Obstructive Azoospermia Risk in the Chinese Population
Cuba: Exploring the History of Admixture and the Genetic Basis of Pigmentation Using Autosomal and Uniparental Mark
Designing a High-Throughput Somatic Mutation Profiling Panel Specifically for Gynaecological Cancers
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