Fine Localization of the Nijmegen Breakage Syndrome Gene to 8q21: Evidence for a Common Founder Haplotype

Author:

Cerosaletti Karen M.,Lange Ethan,Stringham Heather M.,Weemaes Corry M.R.,Smeets Dominique,Sölder B.,Belohradsky B.H.,Taylor A. Malcolm R.,Karnes Pamela,Elliott Alison,Komatsu Kenshi,Gatti Richard A.,Boehnke Michael,Concannon Pat

Publisher

Elsevier BV

Subject

Genetics (clinical),Genetics

Reference30 articles.

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2. Chrzanowska KH, Krajewska-Walasek M, Bernatowska E, Kostyk E, Midro AT, Metera M, Gregorek H, et al (1997) Polish patients with Nijmegen breakage syndrome: clinical and genetic studies. Paper presented at the 7th Ataxia-Telangiectasia Workshop. Clermont-Ferrand, France, November 22–24

3. A chromosomal breakage syndrome with profound immunodeficiency;Conley;Blood,1986

4. Cooper PR, Nowak NJ, Higgins MJ, Simpson SA, Taylor AMR, de Jong PJ, Shows TB (1997) Generation of a high resolution sequence-ready transcription map of the ataxia telangiectasia (A-T) variant, Nijmegen breakage syndrome, region in 8q21. Paper presented at the American Society of Human Genetics 47th annual meeting. Baltimore, October 28–November 1

5. ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndrome;Curry;Am J Hum Genet,1989

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