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The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, maps to a 1-cM interval on chromosome 8q21SAAR, K; CHRZANOWSKA, K. H; STUMM, M et al.American journal of human genetics. 1997, Vol 60, Num 3, pp 605-610, issn 0002-9297Article

HYPERSENSITIVITY TO IONIZING RADIATION, IN VITRO, IN A NEW CHROMOSOMAL BREAKAGE DISORDER, THE NIJMEGEN BREAKAGE SYNDROMETAALMAN RDFM; JASPERS NGJ; SCHERERES JMJC et al.1983; MUTATION RESEARCH; ISSN 0027-5107; NLD; DA. 1983; VOL. 112; NO 1; PP. 23-32; BIBL. 2 P.Article

G2 repair in Nijmegen breakage syndrome : G2 duration and effect of caffeine and cycloheximide in control and X-ray irradiated lymphocytesPINCHEIRA, J; BRAVO, M; SANTOS, M. J et al.Clinical genetics. 1998, Vol 53, Num 4, pp 262-267, issn 0009-9163Article

ATM phosphorylation of Nijmegen breakage syndrome protein is required in a DNA damage responseXIAOHUA WU; RANGANATHAN, V; LIVINGSTON, D. M et al.Nature (London). 2000, Vol 405, Num 6785, pp 477-482, issn 0028-0836Article

A NEW CHROMOSOMAL INSTABILITY DISORDER: THE NIJMEGEN BREAKAGE SYNDROMEWEEMAES CMR; HUSTINX TWJ; SCHERES JMJC et al.1981; ACTA PAEDIATR. SCAND.; ISSN 0001-656X; SWE; DA. 1981; VOL. 70; NO 4; PP. 557-564; BIBL. 31 REF.Article

Frequency of 657del(5) mutation of the NBS1 gene in the Czech population by polymerase chain reaction with sequence specific primersDRABEK, Jiri; HAJDUCH, Marian; GOJOVA, Libuse et al.Cancer genetics and cytogenetics. 2002, Vol 138, Num 2, pp 157-159, issn 0165-4608, 3 p.Article

Lessons from human progeroid syndromes : AgeingMARTIN, George M; OSHIMA, Junko.Nature (London). 2000, Vol 408, Num 6809, pp 263-266, issn 0028-0836Article

A variant of the Nijmegen breakage syndrome with unusual cytogenetic features and intermediate cellular radiosensitivityTUPLER, R; MARSEGLIA, G. L; STEFANINI, M et al.Journal of medical genetics. 1997, Vol 34, Num 3, pp 196-202, issn 0022-2593Article

Eleven polish patients with microcephaly, immunodeficiency, and chromosomal instability : the Nijmegen breakage syndromeCHRZANOWSKA, K. H; KLEIJER, W. J; JANOWICZ, W et al.American journal of medical genetics. 1995, Vol 57, Num 3, pp 462-471, issn 0148-7299Article

Unusual T cell clones in a patient with NIjmegen breakage syndromeSTOPPA-LYONNET, D; GIRAULT, D; LEDEIST, F et al.Journal of medical genetics. 1992, Vol 29, Num 2, pp 136-137, issn 0022-2593Article

Genetic mapping using microcell-mediated chromosome transfer suggests a locus for Nijmegen breakage syndrome at chromosome 8q21-24MATSUURA, S; WEEMAES, C; OSHIMURA, M et al.American journal of human genetics. 1997, Vol 60, Num 6, pp 1487-1494, issn 0002-9297Article

Chromosome instability with bleomycin and X-ray hypersensitivity in a boy with Nijmegen breakage syndromePEREZ-VERA, P; GONZALEZ-DEL ANGEL, A; MOLINA, B et al.American journal of medical genetics. 1997, Vol 70, Num 1, pp 24-27, issn 0148-7299Article

Radiosensitivity of ataxia-telangiectasia, X-linked agammaglobulinemia, and related syndromes using a modified colony survival assayHUO, Y. K; ZHIJUN WANG; JI-HONG HONG et al.Cancer research (Baltimore). 1994, Vol 54, Num 10, pp 2544-2547, issn 0008-5472Article

Impaired p53-mediated DNA damage response, cell-cycle disturbance and chromosome aberrations in Nijmegen breakage syndrome lymphoblastoid cell linesANTOCCIA, A; STUMM, M; SAAR, K et al.International journal of radiation biology (Print). 1999, Vol 75, Num 5, pp 583-591, issn 0955-3002Article

Is 24-color FISH detection of in-vitro radiation-induced chromosomal aberrations suited to determine individual intrinsic radiosensitivity?KUECHLER, Alma; NEUBAUER, Susann; GRABENBAUER, Gerhard G et al.Strahlentherapie und Onkologie. 2002, Vol 178, Num 4, pp 209-215, issn 0179-7158Article

Functional link between ataxia-telangiectasia and Nijmegen breakage syndrome gene productsSONG ZAO; WENG, Y.-C; SHAY, J. W et al.Nature (London). 2000, Vol 405, Num 6785, pp 473-477, issn 0028-0836Article

Ataxia, ocular telangiectasia, chromosome instability, and Langerhans cell histiocytosis in a patient with an unknown breakage syndromeDI ROCCO, M; ARSLANIAN, A; ROMANENGO, M et al.Journal of medical genetics. 1999, Vol 36, Num 2, pp 159-160, issn 0022-2593Article

Combined immunodeficiency, chromosomal instability, and postnatal growth deficiency in a Japanese girlYAMADA, Masafumi; MATSUURA, Shinya; KOBAYASHI, Kunihiko et al.American journal of medical genetics. 2001, Vol 100, Num 1, pp 9-12, issn 0148-7299Article

Fine localization of the Nijmegen breakage syndrome gene to 8q21: Evidence for a common founder haplotypeCEROSALETTI, K. M; LANGE, E; KOMATSU, K et al.American journal of human genetics. 1998, Vol 63, Num 1, pp 125-134, issn 0002-9297Article

First-trimester prenatal diagnosis of the Nijmegen breakage syndrome and ataxia telangiectasia using an assay of radioresistant DNA synthesisJASPERS, N. G. J; VAN DER KRAAN, M; LISSEN, P. C. M et al.Prenatal diagnosis. 1990, Vol 10, Num 10, pp 667-674, issn 0197-3851, 8 p.Article

Possible new variant of Nijmegen breakage syndromeDER KALOUSTIAN, V. M; KLEIJER, W; EYDOUX, P et al.American journal of medical genetics. 1996, Vol 65, Num 1, pp 21-26, issn 0148-7299Article

ATFresno: a phenotype linking ataxia-telangiectasia with the Nijmegen breakage syndromeCURRY, C. J. R; TSAI, J; HUTCHINSON, H. T et al.American journal of human genetics. 1989, Vol 45, Num 2, pp 270-275, issn 0002-9297Article

Ataxia-telangiectasia and the nijmegen breakage syndrome : Related disorders but genes apartSHILOH, Y.Annual review of genetics. 1997, Vol 31, pp 635-662, issn 0066-4197Article

Nijmegen breakage syndrome gene (NBS1) alterations and its protein (nibrin) expression in human ovarian tumoursPLISIECKA-HAŁASA, J; DANSONKA-MIESZKOWSKA, A; REMBISZEWSKA, A et al.Annals of human genetics. 2002, Vol 66, Num 5-6, pp 353-359, issn 0003-4800, 7 p.Article

Cranial MRI in the Nijmegen breakage syndromeBEKIESINSKA-FIGATOWSKA, M; CHRZANOWSKA, K. H; SIKORSKA, J et al.Neuroradiology (Berlin. Print). 2000, Vol 42, Num 1, pp 43-47, issn 0028-3940Article

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