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Germline CHEK2 Gene Mutations in Hereditary Breast Cancer Predisposition – Mutation Types and their Biological and Clinical Relevance

机译：种系Chek2基因突变遗传性乳腺癌的突变 - 突变类型及其生物学和临床相关性

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Petra Kleiblová; Lenka Stolařová; Kateřina Křížová; Filip Lhota; Hojný Jan; Petra Zemánková; Ondřej Havránek; Michal Vočka; Marta Černá; Klára Lhotová; Marianna Borecká; Markéta Janatová; Jana Soukupová; Jan Ševčík; Martina Zimovjanová; Jaroslav Kotlas; Aleš Panczak; Kamila Veselá; Jana Červenková; Michaela Schneiderová; Monika Burócziová; Kamila Burdová; Viktor Stránecký; Lenka Foretová; Eva Macháčková; Spiros Tavandzis; Stanislav Kmoch; Libor Macůrek; Zdeněk Kleibl;
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1. Germline mutations of renal cancer predisposition genes and clinical relevance in Chinese patients with sporadic, early‐onset disease [J] . Wu Junlong, Wang Hongkai, Ricketts Christopher J., Cancer: A Journal of the American Cancer Society . 2019,第7期

机译：中国散发性早发病患者肾癌易感性基因的种系突变和临床关联
2. BRCA hereditary breast and/or ovarian cancer syndromes: a study of 18 patients with deleterious germline mutations in RAD51C , BARD1 , BRIP1 , PALB2 , MUTYH , or CHEK2 [J] . J. Kenneth Schoolmeester, Ann M. Moyer, McKinsey L. Goodenberger, Human Pathology . 2017,第期

机译：BRCA遗传性乳腺和/或卵巢癌综合征：RAD51C，BARD1，BRIP1，PALB2，MUTYH或CHEK2患者18例有害种系突变患者的研究
3. 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
4. Spectropolarimetric comparison of molecular-genetic study of BRCA1 gene mutation types in patients with breast cancer and their relatives [C] . O.P.Peresunko, T.V.Kruk, K.M.Chala, International Conference on Correlation Optics . 2020

机译：BRCA1基因突变类型在乳腺癌及其亲属患者中BRCA1基因突变类型的分子遗传学研究
5. Characterization of germline CHEK2 mutations in African-American women at high risk for hereditary breast cancer. [D] . Hill, Janell Glennette. 2009

机译：遗传性乳腺癌高风险的非裔美国女性生殖系CHEK2突变的表征。
6. Detection of Germline Mutations in Breast Cancer Patients with Clinical Features of Hereditary Cancer Syndrome Using a Multi-Gene Panel Test [O] . Hee-Chul Shin, Han-Byoel Lee, Tae-Kyung Yoo, 2020

机译：用多基因面板试验检测乳腺癌患者乳腺癌癌症患者临床特征的临床特征
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

Germline CHEK2 Gene Mutations in Hereditary Breast Cancer Predisposition – Mutation Types and their Biological and Clinical Relevance

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