Case Series: Clinical Significance of Heterozygous Pathogenic RTEL1 Variants Identified via Routine Clinical Genetic Diagnostics. - Wedge E; Rasmussen AØ; Borgwardt L; Cowland JB; Grønbæk K; Issa II; Friis LS; Andersen MK; Hvidbjerg MS; Jelsig AM (American journal of medical genetics. Part A, 2026)