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机译:鉴定BRCA1 / 2阴性,高风险,遗传性乳腺癌和/或卵巢癌患者的病原变体:高频率的FANCM致病变种
Hannover Med Sch Dept Human Genet Hannover Germany;
Hannover Med Sch Dept Human Genet Hannover Germany;
Hannover Med Sch Dept Human Genet Hannover Germany;
Hannover Med Sch Dept Human Genet Hannover Germany;
Hannover Med Sch Dept Human Genet Hannover Germany;
Hannover Med Sch Dept Human Genet Hannover Germany;
Hannover Med Sch Res Core Unit Genom Hannover Germany;
Hannover Med Sch Dept Obstet &
Gynaecol Hannover Germany;
Hannover Med Sch Dept Human Genet Hannover Germany;
Hannover Med Sch Dept Human Genet Hannover Germany;
Hannover Med Sch Dept Human Genet Hannover Germany;
Tech Univ Dresden Fac Med Carl Gustav Carus Inst Clin Genet Dresden Germany;
Tech Univ Dresden Fac Med Carl Gustav Carus Inst Clin Genet Dresden Germany;
Hannover Med Sch Dept Human Genet Hannover Germany;
Hannover Med Sch Dept Human Genet Hannover Germany;
Hannover Med Sch Dept Human Genet Hannover Germany;
Hannover Med Sch Dept Human Genet Hannover Germany;
Hannover Med Sch Dept Human Genet Hannover Germany;
multi gene panel NGS; comparative genomic hybridization; hereditary breast and ovarian cancer; Nanopore Oxford sequencing;
机译:鉴定BRCA1 / 2阴性,高风险,遗传性乳腺癌和/或卵巢癌患者的病原变体:高频率的FANCM致病变种
机译:鉴定序列变体患有遗传性乳腺癌和卵巢癌的序列变体?BRCA1和BRCA2阴性乳腺癌和卵巢癌患者
机译:BRCA1 / 2致病种系基因变异妇女饮食,体重管理,身体活动和卵巢癌风险:系统评价
机译:基于基因的证据表明捷克乳腺癌患者的药基因和致癌基因中罕见的致病性变异负担
机译:在遗传癌基因中具有不确定意义的个体的医学决策,以及Chek2致病变异的人
机译:BRCA1 c.4096 + 3A G变体显示遗传性乳腺癌和卵巢癌中致病性BRCA1突变的经典特征但仍具有纯合生存能力
机译:BRCA1 C.4096 + 3A> G变体显示遗传性乳腺癌和卵巢癌的病原BRCA1突变的经典特征,但仍然允许纯合的活力