Very Short Telomeres in the Peripheral Blood of Patients with X-Linked and Autosomal Dyskeratosis Congenita
- 1 March 2001
- journal article
- Published by Elsevier in Blood Cells, Molecules, and Diseases
- Vol. 27 (2) , 353-357
- https://doi.org/10.1006/bcmd.2001.0389
Abstract
No abstract availableKeywords
This publication has 20 references indexed in Scilit:
- Dyskeratosis CongenitaPublished by Elsevier ,2018
- Dyskeratosis congenita in all its formsBritish Journal of Haematology, 2000
- A telomerase component is defective in the human disease dyskeratosis congenitaNature, 1999
- Unexplained aplastic anaemia, immunodeficiency, and cerebellar hypoplasia (Hoyeraal‐Hreidarsson syndrome) due to mutations in the dyskeratosis congenita gene, DKC1British Journal of Haematology, 1999
- X-Linked Dyskeratosis Congenita Is Predominantly Caused by Missense Mutations in the DKC1 GeneAmerican Journal of Human Genetics, 1999
- A Box H/ACA Small Nucleolar RNA-Like Domain at the Human Telomerase RNA 3′ EndMolecular and Cellular Biology, 1999
- Dyskeratosis Congenita (DC) Registry: identification of new features of DCBritish Journal of Haematology, 1998
- X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functionsNature Genetics, 1998
- The box H+ACA snoRNAs carry Cbf5p, the putative rRNA pseudouridine synthaseGenes & Development, 1998
- The Hoyeraal-Hreidarsson syndrome: The fourth case of a separate entity with prenatal growth retardation, progressive pancytopenia and cerebellar hypoplasiaEuropean Journal of Pediatrics, 1995