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Volumn 92, Issue 3-4, 2001, Pages 186-191

High frequency of spontaneous translocations revealed by FISH in cells from patients with the cancer-prone syndromes ataxia telangiectasia and Nijmegen breakage syndrome

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; ATAXIA TELANGIECTASIA; CHROMOSOME ABERRATION; CHROMOSOME PAINTING; CHROMOSOME TRANSLOCATION; CYTOGENETICS; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FREQUENCY; GENE MUTATION; GENETIC ANALYSIS; HETEROZYGOTE; HUMAN; HUMAN CELL; LYMPHOBLASTOID CELL; NIJMEGEN BREAKAGE SYNDROME; PRIORITY JOURNAL;

EID: 0034938838     PISSN: 03010171     EISSN: None     Source Type: Journal    
DOI: 10.1159/000056900     Document Type: Article
Times cited : (61)

References (33)
  • 10
    • 0002256253 scopus 로고    scopus 로고
    • Genes altered by chromosomal translocations in leukemia and lymphomas
    • Vogelstein B, Kinzler KW (eds): The genetic basis of human cancer (McGraw-Hill, New York)
    • (1998) , pp. 109-141
    • Look, A.T.1
  • 11
    • 0004568853 scopus 로고    scopus 로고
    • Detection of radiosensitivity by means of three color FISH
    • Rautenstrauss B, Liehr T (eds): FISH-Technologies (Springer, Heidelberg, in press)
    • (2001) Springer Lab Manual
    • Neubauer, S.1
  • 19
    • 0025268280 scopus 로고
    • An increased risk for malignant neoplasms in heterozygotes for a syndrome of microcephaly, normal intelligence, growth retardation, remarkable facies, immunodeficiency and chromosomal instability
    • (1990) Mutat Res , vol.238 , pp. 321-324
    • Seemanov, E.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.