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5. Eleven Polish patients with microcephaly, immunodeficiency, and chromosomal instability: the Nijmegen breakage syndrome. Chrzanowska KH; Kleijer WJ; Krajewska-Walasek M; Białecka M; Gutkowska A; Goryluk-Kozakiewicz B; Michałkiewicz J; Stachowski J; Gregorek H; Lysón-Wojciechowska G Am J Med Genet; 1995 Jul; 57(3):462-71. PubMed ID: 7545870 [TBL] [Abstract][Full Text] [Related]
6. Patients with an inherited syndrome characterized by immunodeficiency, microcephaly, and chromosomal instability: genetic relationship to ataxia telangiectasia. Jaspers NG; Taalman RD; Baan C Am J Hum Genet; 1988 Jan; 42(1):66-73. PubMed ID: 3337113 [TBL] [Abstract][Full Text] [Related]
7. Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24. Matsuura S; Weemaes C; Smeets D; Takami H; Kondo N; Sakamoto S; Yano N; Nakamura A; Tauchi H; Endo S; Oshimura M; Komatsu K Am J Hum Genet; 1997 Jun; 60(6):1487-94. PubMed ID: 9199571 [TBL] [Abstract][Full Text] [Related]
8. A new chromosomal instability disorder confirmed by complementation studies. Wegner RD; Metzger M; Hanefeld F; Jaspers NG; Baan C; Magdorf K; Kunze J; Sperling K Clin Genet; 1988 Jan; 33(1):20-32. PubMed ID: 3277755 [TBL] [Abstract][Full Text] [Related]
9. Complementation of chromosomal aberrations in AT/NBS hybrids: inadequacy of RDS as an endpoint in complementation studies with immortal NBS cells. Kraakman-van der Zwet M; Overkamp WJ; Jaspers NG; Natarajan AT; Lohman PH; Zdzienicka MZ Mutat Res; 2001 Apr; 485(3):177-85. PubMed ID: 11267829 [TBL] [Abstract][Full Text] [Related]
10. Genetic complementation analysis of ataxia telangiectasia and Nijmegen breakage syndrome: a survey of 50 patients. Jaspers NG; Gatti RA; Baan C; Linssen PC; Bootsma D Cytogenet Cell Genet; 1988; 49(4):259-63. PubMed ID: 3248383 [TBL] [Abstract][Full Text] [Related]
11. Radiosensitivity of ataxia-telangiectasia, X-linked agammaglobulinemia, and related syndromes using a modified colony survival assay. Huo YK; Wang Z; Hong JH; Chessa L; McBride WH; Perlman SL; Gatti RA Cancer Res; 1994 May; 54(10):2544-7. PubMed ID: 8168076 [TBL] [Abstract][Full Text] [Related]
12. Further delineation of the Nijmegen breakage syndrome. Taalman RD; Hustinx TW; Weemaes CM; Seemanová E; Schmidt A; Passarge E; Scheres JM Am J Med Genet; 1989 Mar; 32(3):425-31. PubMed ID: 2786340 [TBL] [Abstract][Full Text] [Related]
13. [Immunodeficiency and chromosome instability]. Weemaes CM; Bakkeren JA; Hustinx TW; van Munster PJ; Scheres JM Tijdschr Kindergeneeskd; 1988 Oct; 56(5):209-12. PubMed ID: 3206518 [TBL] [Abstract][Full Text] [Related]
15. Noncomplementation of radiation-induced chromosome aberrations in ataxia-telangiectasia/ataxia-telangiectasia-variant heterodikaryons. Stumm M; Sperling K; Wegner RD Am J Hum Genet; 1997 May; 60(5):1246-51. PubMed ID: 9150175 [No Abstract] [Full Text] [Related]
16. Complementation analysis in ataxia telangiectasia: fibroblast-lymphoblastoid cell heterokaryon assay by radiation-induced chromosome aberrations. Chen P; Kidson C Cytogenet Cell Genet; 1993; 64(1):9-11. PubMed ID: 8508684 [TBL] [Abstract][Full Text] [Related]
17. Variants of Nijmegen breakage syndrome and ataxia telangiectasia. Weemaes CM; Smeets DF; Horstink M; Haraldsson A; Bakkeren JA Immunodeficiency; 1993; 4(1-4):109-11. PubMed ID: 7513225 [TBL] [Abstract][Full Text] [Related]
18. Unusual T cell clones in a patient with Nijmegen breakage syndrome. Stoppa-Lyonnet D; Girault D; LeDeist F; Aurias A J Med Genet; 1992 Feb; 29(2):136-7. PubMed ID: 1613764 [TBL] [Abstract][Full Text] [Related]
19. Hypersensitivity to ionizing radiation, in vitro, in a new chromosomal breakage disorder, the Nijmegen Breakage Syndrome. Taalman RD; Jaspers NG; Scheres JM; de Wit J; Hustinx TW Mutat Res; 1983 Feb; 112(1):23-32. PubMed ID: 6828038 [TBL] [Abstract][Full Text] [Related]
20. Nijmegen breakage syndrome. van der Burgt I; Chrzanowska KH; Smeets D; Weemaes C J Med Genet; 1996 Feb; 33(2):153-6. PubMed ID: 8929954 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]