A scalable EHR-based approach for phenotype discovery and variant interpretation for hereditary cancer genes
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A scalable EHR-based approach for phenotype discovery and variant interpretation for hereditary cancer genes

Zeng C, Bastarache L. A, Tao R, Venner E, Hebbring S, Andujar J. D, Bland S. T, Crosslin D. R, Pratap S, Cooley A, Pacheco J. A, Christensen K. D, Perez E. F, Blout Zawatsky C. L, Witkowski L, Zouk H, Weng C, Leppig K. A, Sleiman P. M. A, Hakonarson H, Williams M, Luo Y, Jarvik G. P, Green R. C, Chung W, Gharavi A. G, Lennon N. J, Rehm H. L, Gibbs R. A, Peterson J. F, Roden D. M, Wiesner G. L, Denny J. C.

DOI: doi:10.1101/2021.03.18.21253763
Date of Release: 2021-03-24

Genetic & Genomic Medicine

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