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BMC Medical Genetics
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141 The rs1990760 polymorphism within the IFIH1 locus is not associated with Graves' disease, Hashimoto's thyroiditis and Addison's disease.
142 Association of vitamin D receptor polymorphisms with the risk of prostate cancer in the Han population of Southern China.
143 Characterisation of CYP2C8, CYP2C9 and CYP2C19 polymorphisms in a Ghanaian population.
144 Analyses of associations between three positionally cloned asthma candidate genes and asthma or asthma-related phenotypes in a Chinese population.
145 Further analysis of previously implicated linkage regions for Alzheimer's disease in affected relative pairs.
146 Confirmation of the genetic association of CTLA4 and PTPN22 with ANCA-associated vasculitis.
147 Relationship of circulating cell-free DNA levels to cell-free fetal DNA levels, clinical characteristics and laboratory parameters in preeclampsia.
148 A novel study of Copy Number Variations in Hirschsprung disease using the Multiple Ligation-dependent Probe Amplification (MLPA) technique.
149 Emilin1 gene and essential hypertension: a two-stage association study in northern Han Chinese population.
150 Genetic variation in the NBS1, MRE11, RAD50 and BLM genes and susceptibility to non-Hodgkin lymphoma.
151 Molecular analysis of T-B-NK+ severe combined immunodeficiency and Omenn syndrome cases in Saudi Arabia.
152 PIN1 gene variants in Alzheimer's disease.
153 Voltage-dependent anion channel (VDAC) is involved in apoptosis of cell lines carrying the mitochondrial DNA mutation.
154 ALDH1A2 (RALDH2) genetic variation in human congenital heart disease.
155 PLAUR polymorphisms and lung function in UK smokers.
156 Candidate genetic analysis of plasma high-density lipoprotein-cholesterol and severity of coronary atherosclerosis.
157 Telomere shortening may be associated with human keloids.
158 Variation in cytokine genes can contribute to severity of acetabular osteolysis and risk for revision in patients with ABG I total hip arthroplasty: a genetic association study.
159 Association of APOE polymorphism with chronic kidney disease in a nationally representative sample: a Third National Health and Nutrition Examination Survey (NHANES III) Genetic Study.
160 Suggestive linkage detected for blood pressure related traits on 2q and 22q in the population on the Samoan islands.
 
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