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Comparison of the molecular profile of brain metastases from colorectal cancer and corresponding primary tumors
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
Childhood-onset Leigh syndrome transforming into an episodic weakness phenotype with axonal neuropathy caused by MT-ATP6 mutations
Genetic 3′ UTR variation is associated with human pigmentation characteristics and sensitivity to sunlight
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