X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions-Reference-Cited by-同舟云学术

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X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions

Published:1998-05 Issue:1 Volume:19 Page:32-38
ISSN:1061-4036
Container-title:Nature Genetics
language:en
Short-container-title:Nat Genet

Author:

Heiss Nina S.,Knight Stuart W.,Vulliamy Tom J.,Klauck Sabine M.,Wiemann Stefan,Mason Philip J.,Poustka Annemarie,Dokal Inderjeet

Publisher

Springer Science and Business Media LLC

Subject

Genetics

Link

http://www.nature.com/articles/ng0598-32.pdf

Reference41 articles.

1. Connor, J.M., Gatherer, D., Gray, F.C., Pirrit, L.A. & Affara, N.A. Assignment of the gene for dyskeratosis congenita to Xq28. Hum. Genet. 72, 348–351 (1986).

2. Arngrimsson, R., Dokal, I., Luzzatto, L. & Connor, J.-M. Dyskeratosis congenita: three additional families show linkage to a locus in Xq28. J. Med. Genet. 30, 618–619 (1993).

3. Drachtman, R.A. & Alter, B.P. Dyskeratosis congenita: Clinical and genetic heterogeneity: Report of a a new case and review of the literature. Am. J. Pediatr. Hemat Oncol. 14, 297–304 (1992).

4. Dokal, I. Dyskeratosis congenita: An inherited bone marrow failure syndrome. Br. J. Haematol. 92, 775–779 (1996).

5. Dokal, I. & Luzzatto, L., Congenita is a chromosomal instability disorder. Leukemia and Lymphoma 15, 1–7 (1994).

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