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High throughput germline mutation screening for hereditary breast cancer in Southern Chinese patients by massively parallel DNA sequencing

机译：中国南方患者遗传性乳腺癌高通量种系突变筛选大规模平行DNa测序

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Session: Genetics: Poster presentation

机译：会议：遗传学：海报展示

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Au, CH; Ho, DN; Ma, ESK; Kwong, A; Law, FBF; Chan, TL; Wong, ATC; Ip, BK;
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年度 2013
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正文语种 eng
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1. Screening for germline BRCA1, BRCA2, TP53 and CHEK2 mutations in families at-risk for hereditary breast cancer identified in a population-based study from Southern Brazil [J] . Palmero Edenir Inêz, Alemar Bárbara, Schüler-Faccini Lavínia, Genetics and molecular biology: publication of the Sociedade Brasileira de Genetica . 2016,第2期

机译：来自巴西南部的一项基于人群的研究确定了遗传性乳腺癌高危家庭的生殖系BRCA1，BRCA2，TP53和CHEK2突变
2. Screening for germline BRCA1 , BRCA2 , TP53 and CHEK2 mutations in families at-risk for hereditary breast cancer identified in a population-based study from Southern Brazil [J] . Patricia Lisb?a Izetti Ribeiro, Patricia Ashton-Prolla, Lavínia Schüler-Faccini, Genetics and molecular biology: publication of the Sociedade Brasileira de Genetica . 2016,第2期

机译：在巴西南部一项基于人群的研究中确定了遗传性乳腺癌风险家庭中的种系BRCA1，BRCA2，TP53和CHEK2突变
3. Spectrum of PALB2 PALB2 germline mutations and characteristics of PALB2 PALB2 ‐related breast cancer: Screening of 16,501 unselected patients with breast cancer and 5890 controls by next‐generation sequencing [J] . Cancer: A Journal of the American Cancer Society . 2020,第14期

机译：PALB2 PALB2种系突变和PALB2 PALB2-相关乳腺癌特征的光谱：通过下一代测序筛选乳腺癌和5890患者的16,501名未选择的患者和5890个对照
4. Hereditary Cancer Screening Using Targeted Next Generation Sequencing on DNA Extracted from Human Buccal Cells [C] . Mark Dobbs, Pankaj Sethi, Ivan Rueda, International Molecular Medicine Tri-Conference. . 2016

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5. Characterization of germline CHEK2 mutations in African-American women at high risk for hereditary breast cancer. [D] . Hill, Janell Glennette. 2009

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6. Identification of BRCA1/2 Founder Mutations in Southern Chinese Breast Cancer Patients Using Gene Sequencing and High Resolution DNA Melting Analysis [O] . Ava Kwong, Enders Kai On Ng, Chris Lei Po Wong, -1

机译：中国南方乳腺癌患者BRCa1 / 2突变创始人鉴定利用基因测序和高分辨率DNa解链分析
7. Screening for germline BRCA1, BRCA2, TP53 and CHEK2 mutations in families at-risk for hereditary breast cancer identified in a population-based study from Southern Brazil [O] . Edenir Inêz Palmero, Bárbara Alemar, Lavínia Schüler-Faccini, 2016

机译：在巴西南部的一项基于人群的研究中发现的遗传性乳腺癌家系中种系BRCa1，BRCa2，Tp53和CHEK2突变的筛查

High throughput germline mutation screening for hereditary breast cancer in Southern Chinese patients by massively parallel DNA sequencing

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