المؤلفون: Taichi Hagio, Seiichi Mori, Sayuri Amino, Takeshi Nakajima, Tetsuo Noda, Tomoko Kaneyasu, Seigo Nakamura, Masaaki Matsuura, Tomo Osako, Noriko Yaguchi, Toru Hirota, Eri Nakashima, Dai Kitagawa, Takayuki Ueno, Reiko Yoshida, Osamu Gotoh, Norio Tanaka, Shinji Ohno, Yoshio Miki, Shunji Takahashi

المصدر: Cancer Science

مصطلحات موضوعية: Genetics, Genomics and Proteomics, 0301 basic medicine, Cancer Research, variants of uncertain significance, DNA Mutational Analysis, Datasets as Topic, Ataxia Telangiectasia Mutated Proteins, Loss of heterozygosity, 0302 clinical medicine, Exome, Breast, Homologous Recombination, Mastectomy, Exome sequencing, Genetics, BRCA1 Protein, Lasso logistic regression, General Medicine, Middle Aged, hereditary breast and ovarian cancer syndrome, Oncology, homologous recombination deficiency, 030220 oncology & carcinogenesis, Female, Original Article, Fanconi Anemia Complementation Group N Protein, Adult, PALB2, Breast Neoplasms, Biology, 03 medical and health sciences, Germline mutation, Breast cancer, Exome Sequencing, Biomarkers, Tumor, BRCAness, medicine, Humans, Genetic Predisposition to Disease, Genetic Testing, Allele, Germ-Line Mutation, Aged, BRCA2 Protein, Models, Genetic, Original Articles, medicine.disease, Checkpoint Kinase 2, 030104 developmental biology, Ovarian cancer

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::376ea8b3a6a9aaa8a778b0ed5b65fb15
https://doi.org/10.1111/cas.14803

المؤلفون: Yoshio Miki, Yuri Sato, Sachio Nomura, Eri Nakashima, Shinji Ohno, Masami Arai, Reiko Yoshida, Mizuho Kita, Takuji Iwase, Yasue Adachi, Yuumi Ashihara, Dai Kitagawa, Katsutoshi Sato, Mio Koyasu

المصدر: Cancer Science. 108:2287-2294

مصطلحات موضوعية: 0301 basic medicine, Proband, Genetics, Cancer Research, Mutation, business.industry, PALB2, General Medicine, medicine.disease_cause, medicine.disease, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, Breast cancer, Oncology, 030220 oncology & carcinogenesis, Cancer research, Medicine, RAD51C, Missense mutation, Mutation frequency, skin and connective tissue diseases, business, Ovarian cancer

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::f3bef46b755b36ca4407250508a32505
https://doi.org/10.1111/cas.13350