1.4 Mb candidate gene region for X linked dyskeratosis congenita defined by combined haplotype and X chromosome inactivation analysis.

Author:

Knight S W,Vulliamy T J,Heiss N S,Matthijs G,Devriendt K,Connor J M,D'Urso M,Poustka A,Mason P J,Dokal I

Publisher

BMJ

Subject

Genetics (clinical),Genetics

Reference23 articles.

1. Dyskeratosis congenita: clinical and genetic heterogeneity. Report of a new case and review of the literature;Drachtman, R.A.; Alter, B.P.;Am J Pediatr Hematol Oncol,1992

2. Dyskeratosis congenita: an inherited bone marrow failure syndrome;Dokal, I.;BrJ Haematol,1996

3. Initial analysis from the dyskeratosis congenita registry (DCR);Knight, S.W.; Vulliamy, T.; Mason, P.J.;Blood,1997

4. Chromosomal breakage analysis in dyskeratosis congenita peripheral blood lymphocytes;Coulthard, S.; Chase, A.; Pickard, J.,1997

5. Assignment of the gene for dyskeratosis congenita to Xq28;Connor, J.M.; Gatherer, D.; Gray, F.C.;Hum Genet,1986

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