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  • Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13
  • Genetic sequence variants and the development of secondary primary cancers in patients with head and neck cancers
  • Mutations of TFAP2B in congenital heart disease patients in Mysore, south India
  • High-throughput genotyping in osteosarcoma identifies multiple mutations in phosphoinositide-3-kinase and other oncogenes
  • SNP association study for backfat and intramuscular fat content in the region between SW2098 and SW1881 on pig chromosome 6
  • Hypomethylation of the 14-3-3? promoter leads to increased expression in non-small cell lung cancer.
  • Validation of Genetic Sequence Variants as Prognostic Factors in Early Stage Head and Neck Squamous Cell Cancer Survival
  • ONCOGENE MUTATION PROFILING OF PEDIATRIC SOLID TUMORS REVEALS SIGNIFICANT SUBSETS OF EMBRYONAL RHABDOMYOSARCOMA AND NEUROBLASTOMA WITH MUTATED GENES IN GROWTH SIGNALING PATHWAYS
  • Genome-Wide Gene-Environment Study Identifies Glutamate Receptor Gene GRIN2A as a Parkinson’s Disease Modifier Gene via Interaction with Coffee
  • Plasma adrenomedullin level is related to a single nucleotide polymorphism in the adrenomedullin gene
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