Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study (Genetics in Medicine, (2019), 21, 5, (1100-1110), 10.1038/s41436-018-0308-x)Ragan Hart,Barbara B. Biesecker,Carrie L. Blout,Kurt D. Christensen,Laura M. Amendola,Katie Bergstrom,Sawona Biswas,Kevin M. Bowling,Laura K. Conlin,Greg M. Cooper,Matthew C. Dulik,Kelly M. East,Jessica Everett,Candice R. Finnila,Arezou A. Ghazani,Marian J. Gilmore,Katrina A.B. Goddard,Gail P. Jarvik,Jennifer J. Johnston,Tia L. Kauffman,Whitley V. Kelley,Joel B. Krier,Katie L. Lewis,Amy L. McGuire,Carmit K. McMullen,Jeffrey Ou,Sharon E. Plon,Heidi L. Rehm,C. Sue Richards,Edward J. Romasko,Ane Miren Sagardia,Nancy B. Spinner,Michelle L. Thompson,Erin Turbitt,Jason L. Vassy,Benjamin S. Wilfond,David L. Veenstra,Jonathan S. Berg,Robert C. Green,Leslie G. Biesecker,Lucia A. HindorffGenetics in Medicine(2019)引用 4|浏览2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