Unusual T cell clones in a patient with Nijmegen breakage syndrome.

Author:

Stoppa-Lyonnet D,Girault D,LeDeist F,Aurias A

Publisher

BMJ

Subject

Genetics(clinical),Genetics

Reference7 articles.

1. Taalman RDFM. A new chromosomal instability disorder: the Nijmegen breakage syndrome;Weemaes, C.M.R.; Hustinx, T.W.J.; Scheres, J.M.J.C.; Van Munster, P.J.J.; Bakkeren, J.A.J.M.;Acta Paediatr Scand,1981

2. A new chromosomal instability disorder confirmed by complementation studies;Wegner, R.D.; Metzger, M.; Hanefeld, F.;Clin Genet,1988

3. Patients with an inherited syndrome characterized by immunodeficiency, microcephaly, and chromosomal instability: genetic relationship to ataxia telangiectasia;Jaspers, N.G.J.; Taalman, R.D.F.M.; Baan, C.;Am J Hum Genet,1988

4. Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients;Jaspers, N.G.J.; Gatti, R.A.; Baan, C.; Linssen, P.C.M.L.; Bootsma, D.;Cytogenet Cell Genet,1988

5. Chromosome 11 contains genes for the three most common complementation groups of ataxia telangiectasia: a consortium report;Gatti, R.A.; Chessa, L.; McConville, C.;Am J Hum Genet,1990

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