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International Journal of Human Genetics最新文献

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COMTval158met Gene Polymorphism Correlation with Prenatal Anxiety and Labor Analgesia COMTval158met基因多态性与产前焦虑和分娩镇痛的相关性
IF 0.1 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2020-07-13 DOI: 10.31901/24566330.2020/20.03.756
Y. Xiaohong
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引用次数: 0
Impact of Tobacco on Proinflammatory IL1α Protein Expression in Smokers and Chewing Tobacco Users: A Novel Approach towards Protein-Ligand Incorporated Docking Analysis 烟草对吸烟者和咀嚼烟草使用者促炎il - 1α蛋白表达的影响:一种蛋白质-配体结合对接分析的新方法
IF 0.1 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2020-07-13 DOI: 10.31901/24566330.2020/20.02.754
Poulami Majumder
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引用次数: 0
Mitochondrial Dysfunction and PINK1Gene Mutation: In Parkinson‘sDisease (PD) 帕金森病(PD)的线粒体功能障碍和pink1基因突变
IF 0.1 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2020-07-05 DOI: 10.31901/24566330.2020/20.04.766
A. Anand
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引用次数: 0
Genetics of Chronic Obstructive Pulmonary Disease - A Literature Review 慢性阻塞性肺疾病的遗传学——文献综述
IF 0.1 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2020-07-02 DOI: 10.31901/24566330.2020/20.03.757
T. Sangeetha
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引用次数: 0
Thrombocytopenia and Lung Disorder - Interconnected? - An Overview 血小板减少症和肺部疾病-相互关联?-概述
IF 0.1 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2020-07-02 DOI: 10.31901/24566330.2020/20.03.758
M. Kaviya
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引用次数: 0
Regulator of Chromosome Condensation 2 is a Poor Prognostic Factor in Hepatocellular Carcinoma 染色体凝结2调节因子是肝癌预后不良的因素
IF 0.1 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2020-06-25 DOI: 10.31901/24566330.2020/20.03.763
Zhe-Long Liang
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引用次数: 0
Expressions of CD Markers, Anti-NMDAR and Anti-GAD Antibodies, and Serum Levels of immunoglobulins in Children with Autoimmune Encephalitis 儿童自身免疫性脑炎CD标志物、抗NMDAR和抗GAD抗体的表达及血清免疫球蛋白水平
IF 0.1 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2020-06-11 DOI: 10.31901/24566330.2020/20.02.753
Shiping Wang
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引用次数: 0
Comparing the SCN5A Gene Sequence and Expression in Three Different Brugada Syndrome Profiles of Patients: New Insights for Genotype-Phenotype Correlation 比较三种不同Brugada综合征患者SCN5A基因序列和表达:基因型-表型相关性的新见解
IF 0.1 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2020-06-05 DOI: 10.31901/24566330.2020/20.03.727
A. Khelil
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引用次数: 0
Molecular Basis of cKit Mutation in Recurrent Gastrointestinal Stromal Tumour (GIST): A Case Report from India 复发性胃肠道间质瘤(GIST)cKit突变的分子基础:一例来自印度的病例报告
IF 0.1 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2020-04-15 DOI: 10.31901/24566330.2020/12.02.749
S. M.L
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引用次数: 0
VEGFR2 Gene Variation is Associated with Ovarian Hyper Stimulation Syndrome VEGFR2基因变异与卵巢过度刺激综合征相关
IF 0.1 4区 生物学 Q4 GENETICS & HEREDITY Pub Date : 2020-04-15 DOI: 10.31901/24566330.2020/20.02.744
S. Tural
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引用次数: 1
期刊
International Journal of Human Genetics
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