机译:单倍型共享为芬兰的微尺度人口历史和疾病提供了见解
Analytic and Translational Genetics Unit Massachusetts General Hospital;
Analytic and Translational Genetics Unit Massachusetts General Hospital;
Institute for Molecular Medicine Finland (FIMM) University of Helsinki;
Analytic and Translational Genetics Unit Massachusetts General Hospital;
Institute for Molecular Medicine Finland (FIMM) University of Helsinki;
Analytic and Translational Genetics Unit Massachusetts General Hospital;
National Institute for Health and Welfare of Finland;
Program in Medical and Population Genetics Broad Institute of Harvard and MIT;
Program in Medical and Population Genetics Broad Institute of Harvard and MIT;
Institute for Molecular Medicine Finland (FIMM) University of Helsinki;
Institute for Molecular Medicine Finland (FIMM) University of Helsinki;
Almazov National Medical Research Centre;
Heart Center Foundation Drug Research Centre;
Almazov National Medical Research Centre;
Center for Life Course Health Research Faculty of Medicine University of Oulu;
Estonian Genome Center University of Tartu;
Institute for Molecular Medicine Finland (FIMM) University of Helsinki;
Lund University Diabetes Centre Department of Clinical Sciences Lund University CRC Sk?ne;
Research Centre of Applied and Preventive Cardiovascular Medicine University of Turku Turku;
Almazov National Medical Research Centre;
National Institute for Health and Welfare of Finland;
Institute for Molecular Medicine Finland (FIMM) University of Helsinki;
Program in Medical and Population Genetics Broad Institute of Harvard and MIT;
Analytic and Translational Genetics Unit Massachusetts General Hospital;
Institute for Molecular Medicine Finland (FIMM) University of Helsinki;
Institute for Molecular Medicine Finland (FIMM) University of Helsinki;
Analytic and Translational Genetics Unit Massachusetts General Hospital;
Finland; haplotypes; population genetics; rare variants; human history;
机译:单倍型共享为芬兰的微尺度人口历史和疾病提供了见解
机译:北欧棕熊(Ursus arctos)的Y染色体单倍型分布提供了对种群历史和恢复的了解
机译:在芬兰人群中,ESR1基因变异,单倍型以及冠心病和缺血性中风的风险:一项前瞻性随访研究。
机译:基于单倍型的分类剂,以预测对复杂疾病的单个易感性:多发性硬化的一个例子
机译:分析四个群体中一心一意的同源性2位点的连锁不平衡和单倍型,作为分析复杂遗传病中候选基因座的模型。
机译:单倍型共享提供对芬兰小规模人口史和疾病的见解
机译:单倍型共享在芬兰的微尺度人口历史和疾病中提供见解