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- Auerbach A. D., Rogatko A., Schroeder-Kurth T. M. International Fanconi Anemia Registry: relation of clinical symptoms to diepoxybutane sensitivity. Blood. 1989 Feb;73(2):391–396. [PubMed] [Google Scholar]
- Davidson H. R., Connor J. M. Dyskeratosis congenita. J Med Genet. 1988 Dec;25(12):843–846. doi: 10.1136/jmg.25.12.843. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dokal I. Dyskeratosis congenita: an inherited bone marrow failure syndrome. Br J Haematol. 1996 Mar;92(4):775–779. doi: 10.1046/j.1365-2141.1996.355881.x. [DOI] [PubMed] [Google Scholar]
- Singh K., Kolalapudi S. Dyskeratosis congenita: report of the first case from India. J Dermatol. 1986 Feb;13(1):54–58. doi: 10.1111/j.1346-8138.1986.tb02900.x. [DOI] [PubMed] [Google Scholar]
- Sirinavin C., Trowbridge A. A. Dyskeratosis congenita: clinical features and genetic aspects. Report of a family and review of the literature. J Med Genet. 1975 Dec;12(4):339–354. doi: 10.1136/jmg.12.4.339. [DOI] [PMC free article] [PubMed] [Google Scholar]

