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CrossRef Text and Data Mining |
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Detection of Germline Mutations in Breast Cancer Patients with Clinical Features of Hereditary Cancer Syndrome Using a Multi-Gene Panel Test |
Hee-Chul Shin, Han-Byoel Lee, Tae-Kyung Yoo, Eun-Shin Lee, Ryong Nam Kim, Boyoung Park, Kyong-Ah Yoon, Charny Park, Eun Sook Lee, Hyeong-Gon Moon, Dong-Young Noh, Sun-Young Kong, Wonshik Han |
Cancer Research and Treatment. 2020;52(3):697-713. Published online 2020 February 4 DOI: https://doi.org/10.4143/crt.2019.559 |
Detection of Germline Mutations in Breast Cancer Patients with Clinical Features of Hereditary Cancer Syndrome Using a Multi-Gene Panel Test Sequence-based detection of mutations in cadherin 1 to determine the prevalence of germline mutations in patients with invasive lobular carcinoma of the breast Use of multi gene-panel testing to detect hereditary breast cancer gene variants in patients attending to a breast cancer clinic, Peradeniya, Sri Lanka HER2 Testing in Breast and Gastric Cancer with CDH1 Germline Mutations High Prevalence of Germline Mutations in Cancer Susceptibility Genes in Thai Patients with Clinical Spectrum of Hereditary Breast-Ovarian Cancer Syndrome Psychological and health behaviour outcomes following multi-gene panel testing for hereditary breast and ovarian cancer risk: a mini-review of the literature Clinical Features of Breast Cancer in South Korean Patients with Germline TP53 Gene Mutations BRCA1 andBRCA2 germline mutations in Japanese with hereditary breast cancer families Germline MUTYH gene mutations are not frequently found in unselected patients with papillary breast carcinoma Germline mutations in theRB1 gene in patients with hereditary retinoblastoma |
This metadata service is kindly provided by CrossRef from May 29, 2014. Cancer Res Treat has participated in CrossRef Text and Data Mining service since October 29, 2014. |