The identification of pathogenic variants in BRCA1/2 negative, high risk, hereditary breast and/or ovarian cancer patientsJ. L. van Luttikhuizen,S. Schubert,B. Auber, G. Schmidt,W. Hofmann, J. Penkert,C. F. Davenport, U. Hille-Betz, L. Wendeburg, J. Bublitz, M. Tauscher,K. Hackmann, E. Schroeck,C. Scholz, H. Wallaschek, B. Schlegelberger,T. Illig,D. SteinemannEUROPEAN JOURNAL OF HUMAN GENETICS（2019）引用 43|浏览16暂无评分AI 理解论文溯源树样例生成溯源树，研究论文发展脉络Chat Paper正在生成论文摘要
