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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

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

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BRCA1 andBRCA2 germline mutations in Japanese with hereditary breast cancer families

Takashi Fukutomi, Toshikazu Ushijima, Rie Inoue, Sadako Akashitanaka, Takeshi Nanasawa, Hitoshi Tsuda

Breast Cancer. 1997;4(4):256-258

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Sequence-based detection of mutations in cadherin 1 to determine the prevalence of germline mutations in patients with invasive lobular carcinoma of the breast

Allyson L Valente, Seth Rummel, Craig D Shriver, Rachel E Ellsworth

Hereditary Cancer in Clinical Practice. 2014;12(1):

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Novel germline CDK4 mutations in patients with head and neck cancer

Maimoona Sabir, Ruqia Mehmood Baig, Ishrat Mahjabeen, Mahmood Akhtar Kayani

Hereditary Cancer in Clinical Practice. 2012;10(1):

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O-39. Better survival and distinguishing pathological features of breast cancer in patients with BRCA-1 germline mutations

European Journal of Cancer Supplements. 2005;3(1):13

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Multi-gene panel testing for hereditary cancer predisposition in unsolved high-risk breast and ovarian cancer patients

Beth Crawford, Sophie B. Adams, Taylor Sittler, Jeroen van den Akker, Salina Chan, Ofri Leitner, Lauren Ryan, Elad Gil, Laura van ’t Veer

Breast Cancer Research and Treatment. 2017;163(2):383-390

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Germline mutations in theRB1 gene in patients with hereditary retinoblastoma

Zaoxia Liu, Yue Song, Britta Bia, John K. Cowell

Genes, Chromosomes and Cancer. 1995;14(4):277-284

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Novel germline mutations in BRCA2 gene among 96 hereditary breast and breast–ovarian cancer families from Kerala, South India

Vani Syamala, Leelakumari Sreeja, Volga S. Syamala, B. Vinodkumar, Praveenkumar B. Raveendran, Hariharan Sreedharan, Ratheesan Kuttappan, Lekshmi Balakrishnan, Ravindran Ankathil

Journal of Cancer Research and Clinical Oncology. 2007;133(11):867-874

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Germline MUTYH gene mutations are not frequently found in unselected patients with papillary breast carcinoma

Ewout P Boesaard, Ingrid P Vogelaar, Peter Bult, Carla AP Wauters, J Han JM van Krieken, Marjolijn JL Ligtenberg, Rachel S van der Post, Nicoline Hoogerbrugge

Hereditary Cancer in Clinical Practice. 2014;12(1):

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A screen for germline mutations in the gene encoding CCCTC-binding factor (CTCF) in familial non-BRCA1/BRCA2 breast cancer

Xiao-Lei Zhou, Barbro Werelius, Annika Lindblom

Breast Cancer Research. 2004;6(3):

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