PCHD-003 搜索结果

小柴みなみ[NYGW-002]发行于2014-10-25时长120分钟出品商是豊彦,NYGW-002作品种子搜索下载,加藤真琴[PCHD-003]发行于2014-10-25时长121分钟出品商是豊彦,PCHD-003作品种子搜索下载

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型号: PAC-003 品牌: Powerlet 封装: - 批次: - 数据手册: - 描述: CBL ASSY MULTIMETER 购买数量: 库存:100 最小起订量: 1最小递增量: 1 数量 单价 1 12.3025 请发送询价,我们将立即回复。 产品信息 参数信息 用户指南 MfrPowerlet Series- ...

12%; P<.01) and PON1/AB (54% vs. 40%; P< .01) genotypes and significantly lower frequency of the PON1/AA genotype (27% vs. 48%; P<.0001) than was seen in controls. The age- and sex-adjusted ORs for the development of CHD in the PON1*B carriers (AB and BB genotypes) ...

As compared to normotensives, both HT and CHD-patients had lower cortisol concentrations during the day (HT-vs.-NT: interaction group-by-time: F(3.83,405.78)=2.85,p=.026,η2p=.03,f=0.18); with covariates: F(4.04,407.75)=3.31,p=.011,η2p=.03,f=0.18); CHD-vs.-NT: interaction ...

Results:We found a significant association between hypermethylation ofACTBin peripheral blood and increased risk of CHD (odds ratios (ORs) per +10% methylation: 1.19–1.45,p< 0.013 for nine out of thirteen CpG sites), especially in male subjects and heart failure (HF) patients (ORs per +10...

Code 18a (Part 1) to P701 P003. Code 18a (Part I) P701, Maternal condition, affecting fetus or newborn, diabetes mellitus (conditions in E10-E14) and P003, Maternal condition, affecting fetus or newborn, circulatory disease, (conditions in I00-I99, Q20-Q28). Do not modify the vascul...

Discovery of theCHD3mutation (NM_001005273.2, p.Arg1169Trp) in our index case motivated a search for other de novo mutations in this gene. Studies of large numbers of simplex families with an autistic proband have documented just two single non-synonymous de novo variants inCHD3in probands21...