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  • Genetic and epigenetic methylation defects and implication of the ERMN gene in autism spectrum disorders
  • Point Mutations in Exon 1B of APC Reveal Gastric Adenocarcinoma and Proximal Polyposis of the Stomach as a Familial Adenomatous Polyposis Variant
  • Implementation and Quality Control of Lung Cancer EGFR Genetic Testing by MALDI-TOF Mass Spectrometry in Taiwan Clinical Practice
  • Advances in Blood Typing
  • Two-stage association study to identify the genetic susceptibility of a novel common variant of rs2075290 in ZPR1 to type 2 diabetes
  • Development of nuclear, chloroplast and mitochondrial SNP markers for Khayasp.
  • Phase II study of erlotinib plus tivantinib (ARQ 197) in patients with locally advanced or metastatic EGFR mutation-positive non-small-cell lung cancer just after progression on EGFR-TKI, gefitinib or erlotinib
  • Comprehensive population screening in the Ashkenazi Jewish population for recurrent disease-causing variants
  • Silencer of Cytokine Signaling 1 gene is not hypermethylated in diffuse large B-cell lymphoma
  • Multiple and bilateral kidney tumors with clear cells of three different histotypes: A case report withclinicopathologic and molecular study
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