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| Rank | Title | Journal | Year | PubWeight™‹?› |
|---|---|---|---|---|
| 1 | Malignancies and survival patterns in the National Cancer Institute inherited bone marrow failure syndromes cohort study. | Br J Haematol | 2010 | 3.09 |
| 2 | Ocular and orbital manifestations of the inherited bone marrow failure syndromes: Fanconi anemia and dyskeratosis congenita. | Ophthalmology | 2009 | 1.47 |
| 3 | A role for heterochromatin protein 1γ at human telomeres. | Genes Dev | 2011 | 1.22 |
| 4 | Lung transplantation for pulmonary fibrosis in dyskeratosis congenita: Case Report and systematic literature review. | BMC Blood Disord | 2011 | 1.12 |
| 5 | The relationship between DNA methylation and telomere length in dyskeratosis congenita. | Aging Cell | 2011 | 0.88 |
| 6 | The accumulation and not the specific activity of telomerase ribonucleoprotein determines telomere maintenance deficiency in X-linked dyskeratosis congenita. | Hum Mol Genet | 2011 | 0.83 |