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Search Results for: Hereditary Genetics
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Polymorphism in Serotonin Receptor 3B Is Associated with Pain Catastrophizing
Polymorphisms in ESR1 and FLJ43663 are associated with breast cancer risk in the Han population
Polymorphisms in the ERCC1 and XPF Genes and Risk of Breast Cancer in a Chinese Population
Polymorphisms in the superoxidase dismutase genes reveal no association with human longevity in Germans: a case-control association study
Polymorphisms of EpCAM gene and prognosis for non-small-cell lung cancer in Han Chinese
Mutations causing medullary cystic kidney disease type 1 lie in a large VNTR in MUC1 missed by massively parallel sequencing
Mutations in the UQCC1-Interacting Protein, UQCC2, Cause Human Complex III Deficiency Associated with Perturbed Cytochrome b Protein Expression
NAT2 acetylator phenotype, occupation and bladder cancer risk: Results from the EPIC cohort
Nonsynonymous polymorphisms of the PDLIM5 gene association with the occurrence of both bipolar disorder and schizophrenia
Novel A18T and pA29S substitutions in ?-synuclein may be associated with sporadic Parkinson’s disease
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