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Case Reports in Genetics|December 5, 2024
A Case Report on 13q12.3 Microdeletion Syndrome Caused by <i>HMGB1</i> HaploinsufficiencyTing Wen, Brian J Shayota, Lauren Wallace, et al.European Journal of Haematology|February 24, 2023
Clinical utility of targeted next-generation sequencing panel in routine diagnosis of hereditary hemolytic anemia: A national reference laboratory experienceArchana M Agarwal, Valarie McMurty, Adam L Clayton, et al.Pageof 1