Presenting symptoms and long-term survival in head and neck cancer.

Dyskeratosis congenita with a novel genetic variant in the DKC1 gene: a case report.

Donor telomere length and causes of death after unrelated hematopoietic cell transplantation in patients with marrow failure.

Germline mutations in Protection of Telomeres 1 in two families with Hodgkin lymphoma.

Beginning at the ends: telomeres and human disease.

Genome-wide association study identifies the GLDC/IL33 locus associated with survival of osteosarcoma patients.

No association between donor telomere length and outcomes after allogeneic unrelated hematopoietic cell transplant in patients with acute leukemia.

Relationship between plasma 25-hydroxymitamin D and leucocyte telomere length by sex and race in a US study - CORRIGENDUM.

Beyond the triad: Inheritance, mucocutaneous phenotype, and mortality in a cohort of patients with dyskeratosis congenita.

Pregnancy outcomes in mothers of offspring with inherited bone marrow failure syndromes.

Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-up.

Pediatric leukemia susceptibility disorders: manifestations and management.

Progressive reticulate skin pigmentation and anonychia in a patient with bone marrow failure.

Higher-than-expected population prevalence of potentially pathogenic germline TP53 variants in individuals unselected for cancer history.

Baseline Surveillance in Li-Fraumeni Syndrome Using Whole-Body Magnetic Resonance Imaging: A Meta-analysis.