Germline <i>BRCA2</i> mutations detected in pediatric sequencing studies impact parents' evaluation and care.
第一作者:
Michael F,Walsh
第一单位:
Department of Pediatrics, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA.;Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York 10065, USA.
作者:
医学主题词
BRCA1蛋白质(BRCA1 Protein);BRCA2蛋白质(BRCA2 Protein);儿童(Child);儿童, 学龄前(Child, Preschool);基因, BRCA1(Genes, BRCA1);基因, BRCA2(Genes, BRCA2);疾病遗传易感性(Genetic Predisposition to Disease);遗传隐私(Genetic Privacy);基因检测(Genetic Testing);生殖细胞系突变(Germ-Line Mutation);健康知识, 态度, 实践(Health Knowledge, Attitudes, Practice);人类(Humans);男(雄)性(Male);突变(Mutation);双亲(Parents);系谱(Pedigree);序列分析, DNA(Sequence Analysis, DNA)
DOI
10.1101/mcs.a001925
PMID
28655807
发布时间
2022-01-25
基金项目
P30 CA008748/CA/NCI NIH HHS/United States
R01 CA214812/CA/NCI NIH HHS/United States
- 浏览2
Cold Spring Harbor molecular case studies
2017年3卷6期
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