Kayla J Kolbert - JoVE Visualize

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Orphanet Journal of Rare Diseases|May 24, 2024

Diagnostic yield of exome and genome sequencing after non-diagnostic multi-gene panels in patients with single-system diseasesMatheus V M B Wilke, Eric W Klee, Radhika Dhamija, et al.

Mayo Clinic Proceedings|July 2, 2026

Advancing Pulmonary Fibrosis Care: Integrating Genomic Insights Into Clinical PracticeKathryn T Del Valle, Kayla J Kolbert, Kaitlin J Sikkink, et al.

Journal of Translational Medicine|June 23, 2023

Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD)Filippo Pinto E Vairo, Jennifer L Kemppainen, Carolyn R Rohrer Vitek, et al.

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Showing results (1-10 of 3) with videos related to

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Orphanet Journal of Rare Diseases|May 24, 2024

Diagnostic yield of exome and genome sequencing after non-diagnostic multi-gene panels in patients with single-system diseasesMatheus V M B Wilke, Eric W Klee, Radhika Dhamija, et al.

Mayo Clinic Proceedings|July 2, 2026

Advancing Pulmonary Fibrosis Care: Integrating Genomic Insights Into Clinical PracticeKathryn T Del Valle, Kayla J Kolbert, Kaitlin J Sikkink, et al.

Journal of Translational Medicine|June 23, 2023

Implementation of genomic medicine for rare disease in a tertiary healthcare system: Mayo Clinic Program for Rare and Undiagnosed Diseases (PRaUD)Filippo Pinto E Vairo, Jennifer L Kemppainen, Carolyn R Rohrer Vitek, et al.

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