Stranneheim, H., Lagerstedt-Robinson, K., Magnusson, M., Kvarnung, M., Nilsson, D., Lesko, N., . . . Wedell, A. (2021). Integration of whole genome sequencing into a healthcare setting: High diagnostic rates across multiple clinical entities in 3219 rare disease patients. Genome Med.

Stranneheim, Henrik, et al. "Integration of Whole Genome Sequencing Into a Healthcare Setting: High Diagnostic Rates Across Multiple Clinical Entities in 3219 Rare Disease Patients." Genome Med 2021.

Stranneheim, Henrik, et al. "Integration of Whole Genome Sequencing Into a Healthcare Setting: High Diagnostic Rates Across Multiple Clinical Entities in 3219 Rare Disease Patients." Genome Med 2021.