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机译:关于拷贝数变异的基因组关联研究鉴定了11Q11作为结直肠癌候选敏感性变体的损失
Fundación Pública Galega de Medicina Xenómica (FPGMX)-SERGAS Grupo de Medicina Xenómica Complexo;
Bioinformatics Core Group Department of Oncology University of Oxford Oxford United Kingdom;
Wellcome Trust Centre for Human Genetics University of Oxford Oxford United Kingdom NIHR;
Grupo de Medicina Xenómica Centro de Investigación Biomédica en Red de Enfermedades Raras (CIBERer;
Oncology Pharmacy Unit Complejo Hospitalario Universitario of Santiago (CHUS) 15706 Santiago;
Genetics Department Hospital de Santa Creu i Sant Pau 08025 Barcelona Spain;
Pharmacogenetics and Pharmacogenomics Laboratory Servicio de Farmacia Hospital General;
Gastroenterology Department Hospital Do Meixoeiro 36214 Vigo Spain Section of Digestive;
Colorectal Cancer Multidisciplinary Unit Donostia Hospital University of the Basque Country San;
Servicio de Patologia Digestiva Hospital Sant PAu Barcelona 08003 Spain;
Gastroenterology Department Hospital Do Meixoeiro 36214 Vigo Spain;
Division of Molecular Genetic Epidemiology German Cancer Research Centre (DKFZ) Im Neuenheimer;
Gastroenterology Department Hospital Del Mar Barcelona Spain;
Gastroenterology Department Hospital Del Mar Barcelona Spain;
Gastroenterology Department Hospital General de Alicante Alicante Spain;
Section of Digestive Diseases and Nutrition University of Illinois at Chicago Chicago IL United;
Section of Digestive Diseases and Nutrition University of Illinois at Chicago Chicago IL United;
Cancer Prevention and Control Program Catalan Institute of Oncology (ICO) Bellvitge Biomedical;
Department of Gastroenterology Hospital Clínic University of Barcelona Barcelona Spain;
Department of Gastroenterology Hospital Clínic University of Barcelona Barcelona Spain;
Fundación Pública Galega de Medicina Xenómica (FPGMX)-SERGAS Grupo de Medicina Xenómica Complexo;
Fundación Pública Galega de Medicina Xenómica (FPGMX)-SERGAS Grupo de Medicina Xenómica Complexo;
机译:关于拷贝数变异的全基因组关联研究确定11q11缺失是结肠直肠癌的候选易感性变异
机译:一项西班牙人群的大肠癌全基因组关联研究确定了与1p33和8p12大肠癌风险相关的两个变异
机译:一项西班牙人群的大肠癌全基因组关联研究确定了与1p33和8p12大肠癌风险相关的两个变异
机译:基因组 - 范围的协会研究鉴定了DSH猫(ESVE奖获得者)对糖尿病患者易患的新候选基因
机译:全基因组关联映射和玉米拷贝数变异的检测。
机译:在西班牙队列中进行的大肠癌全基因组关联研究确定了与1p33和8p12大肠癌风险相关的两个变异
机译:在西班牙队列中进行的大肠癌全基因组关联研究确定了与1p33和8p12大肠癌风险相关的两个变异