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MDR1 and CYP3A4 genes variants association with clinical response measured on a five-factor model in multiepisodic schizophrenia and related …
Association between prolactin gene polymorphism (–1149 G/T) and hyperprolactinemia in anti-psychotic treated patients with schizophrenia
Methylome analysis for spina bifida shows SOX18 hypomethylation as risk factor with evidence for a complex (epi) genetic interplay to affect neural tube development
Neural substrates of fear conditioning are modulated by GLRB allelic variation: converging evidence from an independent replication
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
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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