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机译:不同人群携带的BRCA1 / 2携带者的BRCA1 / 2结果的家庭交流和BRCA1 / 2检测的家庭摄取。
Cancer Risk Program University of California San Francisco">(1);
University of Michigan Medical School">(2);
Department of Epidemiology and Biostatistics University of California San Francisco">(3);
Cancer Risk Program University of California San Francisco">(1);
Department of Epidemiology and Biostatistics University of California San Francisco">(3);
Department of Anthropology History and Social Medicine University of California San Francisco">(4);
Department of Medicine University of California San Francisco">(5);
University of California San Francisco">(6);
BRCA1; BRCA2; Hereditary breast and ovarian cancer; Family communication; Family testing; Disparities;
机译:不同人群BRCA1 / 2携带者的BRCA1 / 2结果的家庭沟通和BRCA1 / 2检测的家庭接受
机译:患有BRCA1 / 2 BRCA1 / 2或MMR基因突变的家族内部影响及对遗传检测产生遗传检测的证据的心理社会及临床因素
机译:在BRCA1突变携带者中,常见的IGF1 19 CA重复等位基因缺失比在BRCA1家族的非携带者中更为常见。
机译:癌症护理中易感基因测试的功能和质量要求:以约旦的BRCA1 / 2测试为例
机译:阿什肯纳兹犹太人家庭的隔离分析:另一个乳腺癌易感基因的证据,以及BRCA1 / 2突变携带者的癌症风险评估。
机译:DNA测试结果的家庭沟通的耳语游戏视角:先证者与亲戚之间BRCA1 / 2测试结果的沟通过程的回顾性研究
机译:缺乏共同的IGF1 19 Ca-重复等位基因在BRCa1突变携带者中比在来自BRCa1家族的非携带者中更常见。