Loading...
Keywords
Last Name
Institution

Massively parallel identification of functionally consequential noncoding genetic variants in undiagnosed rare disease patients.

McQuerry JA, Mclaird M, Hartin SN, Means JC, Johnston J, Pastinen T, Younger ST. Massively parallel identification of functionally consequential noncoding genetic variants in undiagnosed rare disease patients. Sci Rep. 2022 05 09; 12(1):7576.

View in: PubMed

collapse authors with profiles