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  • High-throughput genetic screening of 51 pediatric cataract genes identifies causative mutations in inherited pediatric cataract in south eastern Australia
  • Exome array analysis identifies variants in SPOCD1 and BTN3A2 that affect risk for gastric cancer
  • Validating the use of STELA to measure placental telomere length
  • Gender differences in the association of ENPP1 polymorphisms with type 2 diabetes in a Chinese population
  • Functional polymorphisms in PD-L1 gene are associated with the prognosis of patients with early stage non-small cell lung cancer
  • Status and future perspectives of single nucleotide polymorphisms (SNPs) markers in farmed fishes: Way ahead using next generation sequencing
  • Congenital skull fracture as a presenting sign of Menkes disease: A case of perinatal diagnosis and early treatment
  • Whole-genome analysis reveals unexpected dynamics of mutant subclone development in a patient with JAK2-V617F-positive chronic myeloid leukemia
  • Efficacy of FOLFOXIRI plus bevacizumab in liver-limited metastatic colorectal cancer: a pooled analysis of clinical studies by Gruppo Oncologico del Nord …
  • Genetic diversity of 71 Y-chromosomal biallelic markers in the Han population living in Southern China
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