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机译:基因和性别的癌症风险和生存在Path_MMR载体中,最高可达75岁:预期林奇综合征数据库的报告
Oslo Univ Hosp Norwegian Radium Hosp Dept Med Genet Oslo Norway;
Univ Helsinki Helsinki Univ Cent Hosp Dept Gastrointestinal Surg Helsinki Finland;
Copenhagen Univ Hosp Clin Res Ctr Danish Hereditary Nonpolyposis Colorectal Canc Re Hvidovre;
Klinikum Univ Munchen Med Klin &
Poliklin 4 Campus Innenstadt Ziemssenstr Germany;
IRCCS Ist Nazl Tumori Milan Unit Hereditary Digest Tract Tumors Milan Italy;
Cent Manchester Univ Hosp NHS Fdn Trust Manchester Ctr Genom Med London England;
Karolinska Inst Dept Mol Med &
Surg Stockholm Sweden;
Royal Melbourne Hosp Colorectal Med &
Genet Melborne Australia;
IDIBELL Inst Catala Oncol Hereditary Canc Program Barcelona Spain;
Univ Groningen Univ Med Ctr Groningen Dept Genet Groningen Netherlands;
Cardiff Univ Sch Med Inst Med Genet Div Canc &
Genet Hth Pk Cardiff S Glam Wales;
Leiden Univ Med Ctr Dept Gastroenterol &
Hepatol Leiden Netherlands;
Newcastle Univ Inst Genet Med Newcastle Upon Tyne Tyne &
Wear England;
Oslo Univ Hosp Norwegian Radium Hosp Inst Canc Res Dept Tumor Biol Oslo Norway;
Oslo Univ Hosp Norwegian Radium Hosp Inst Canc Res Dept Tumor Biol Oslo Norway;
Oslo Univ Hosp Norwegian Radium Hosp Inst Canc Res Dept Tumor Biol Oslo Norway;
Univ Lancaster Dept Math &
Stat Lancaster England;
Isala Clin Dept Gastroenterol &
Hepatol Zwolle Netherlands;
Cent Manchester Univ Hosp NHS Fdn Trust Dept Surg London England;
Univ Med Ctr Dept Clin Genet Leiden Netherlands;
Univ Melbourne Melbourne Sch Populat &
Global Hlth Ctr Epidemiol &
Biostat Parkville Vic;
Cent Manchester Univ Hosp NHS Fdn Trust Manchester Ctr Genom Med London England;
Cent Manchester Univ Hosp NHS Fdn Trust Manchester Ctr Genom Med London England;
Aalborg Univ Hosp Dept Surg Gastroenterol Aalborg Denmark;
Karolinska Inst Karolinska Univ Hosp Div Obstet &
Gyneacol Dept Womens &
Childrens Hlth;
IRCCS Ist Nazl Tumori Milan Unit Hereditary Digest Tract Tumors Milan Italy;
IDIBELL Inst Catala Oncol Hereditary Canc Program Barcelona Spain;
IDIBELL Inst Catala Oncol Hereditary Canc Program Barcelona Spain;
Klinikum Univ Munchen Med Klin &
Poliklin 4 Campus Innenstadt Ziemssenstr Germany;
Univ Helsinki Helsinki Univ Cent Hosp Dept Gastrointestinal Surg Helsinki Finland;
Oslo Univ Hosp Norwegian Radium Hosp Dept Med Genet Oslo Norway;
Royal Melbourne Hosp Colorectal Med &
Genet Melborne Australia;
Cent Finland Hlth Care Dist Dept Educ &
Sci Yvaskyla Finland;
Univ Cattolica Sacro Cuore A Gemelli Fac Med Inst Genom Med Rome Italy;
Univ Eastern Finland Kuopio Finland;
Cardiff Univ Sch Med Inst Med Genet Div Canc &
Genet Hth Pk Cardiff S Glam Wales;
IDIBELL Inst Catala Oncol Hereditary Canc Program Barcelona Spain;
机译:基因和性别的癌症风险和生存在Path_MMR载体中,最高可达75岁:预期林奇综合征数据库的报告
机译:响应响应Dominguez-Valentin M等人。 2019年:癌症风险由基因,年龄和性别在6350年的致病失配修复变体:从前瞻性林奇综合征数据库的调查结果
机译:对Dominguez-Valentin M等人的回应。 2019年:癌症风险由基因,年龄和性别在6350年的致病失配修复变体:从前瞻性林奇综合征数据库的调查结果
机译:糖尿病在印度尼西亚成年人中患有代谢综合征的糖尿病风险肥胖,6年前瞻性队列研究
机译:Lynch综合征患者的修饰基因和对结直肠癌的易感性
机译:原始文章:高达75岁的按基因和性别分类的path_MMR携带者中path_MMR携带者的癌症风险和生存率:前瞻性林奇综合症数据库的报告
机译:path_mmR携带者的癌症风险和存活率基因和性别高达75岁;前瞻性Lynch综合症数据库的报告