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Volumn 98, Issue 1, 1997, Pages 216-218

Childhood acute lymphoblastic leukaemia with ider(21)(q10)t(12;21)(p12;q22): A new recurrent abnormality showing ETV6/CBFA2 fusion

Author keywords

Childhood ALL; Cytogenetics; ETV6 CBFA2; FISH

Indexed keywords

ACUTE LYMPHOBLASTIC LEUKEMIA; ARTICLE; CASE REPORT; CHILDHOOD LEUKEMIA; CHROMOSOME ABERRATION; CHROMOSOME TRANSLOCATION; FLUORESCENCE IN SITU HYBRIDIZATION; HUMAN; HUMAN CELL; MALE; PRESCHOOL CHILD; PRIORITY JOURNAL;

EID: 0030748538     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1997.1652982.x     Document Type: Article
Times cited : (13)

References (12)
  • 1
    • 0030612269 scopus 로고    scopus 로고
    • Deletions of CDKIB and ETV6 in acute myeloid leukemia and myelodysplastic syndromes without cytogenetic evidence of 12p abnormalities
    • in press
    • Andreasson, P., Johansson, B., Arheden, K., Billström, R., Mitelman, F. & Höglund, M. (1997) Deletions of CDKIB and ETV6 in acute myeloid leukemia and myelodysplastic syndromes without cytogenetic evidence of 12p abnormalities. Genes Chromosomes and Cancer. in press.
    • (1997) Genes Chromosomes and Cancer
    • Andreasson, P.1    Johansson, B.2    Arheden, K.3    Billström, R.4    Mitelman, F.5    Höglund, M.6
  • 6
    • 0030056476 scopus 로고    scopus 로고
    • High incidence of TEL/AML1 fusion resulting from a cryptic t(12;21) in childhood B-lineage acute lymphoblastic leukemia in Taiwan
    • Liang, D.C., Chou, T.B., Chen, J.S., Shurtleff, S.A., Rubnitz, J.E., Downing, J.R., Pui, C.H. & Shih, L.Y. (1996) High incidence of TEL/AML1 fusion resulting from a cryptic t(12;21) in childhood B-lineage acute lymphoblastic leukemia in Taiwan. Leukemia, 10, 991-993.
    • (1996) Leukemia , vol.10 , pp. 991-993
    • Liang, D.C.1    Chou, T.B.2    Chen, J.S.3    Shurtleff, S.A.4    Rubnitz, J.E.5    Downing, J.R.6    Pui, C.H.7    Shih, L.Y.8
  • 9
    • 9244221153 scopus 로고    scopus 로고
    • The 12:21 translocation involving TEL and deletion of the other TEL allele: Two frequentiy associated alterations found in childhood acute lymphoblastic leukemia
    • Raynaud, S., Cavé, G., Baens, M., Bastard, C., Cacheux, V., Grosgeorge, J., Guidal-Giraux, C., Guo, C., Vilmer, E., Marynen, P. & Grandchamp, B. (1996) The 12:21 translocation involving TEL and deletion of the other TEL allele: two frequentiy associated alterations found in childhood acute lymphoblastic leukemia. Blood. 87, 2891-2899.
    • (1996) Blood , vol.87 , pp. 2891-2899
    • Raynaud, S.1    Cavé, G.2    Baens, M.3    Bastard, C.4    Cacheux, V.5    Grosgeorge, J.6    Guidal-Giraux, C.7    Guo, C.8    Vilmer, E.9    Marynen, P.10    Grandchamp, B.11
  • 12
    • 13344282725 scopus 로고
    • TEL/AML1 fusion resulting from a cryptic t(12:21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis
    • Shurtleff, S.A., Buijs, A., Behm, F.G., Rubnitz, J.E., Raimondi, S.C., Hancock, M.L., Chan, G.C.-F., Pui, C-H., Grosveld, G. & Downing, J.R. (1995) TEL/AML1 fusion resulting from a cryptic t(12:21) is the most common genetic lesion in pediatric ALL and defines a subgroup of patients with an excellent prognosis. Leukemia. 9, 1985-1989.
    • (1995) Leukemia , vol.9 , pp. 1985-1989
    • Shurtleff, S.A.1    Buijs, A.2    Behm, F.G.3    Rubnitz, J.E.4    Raimondi, S.C.5    Hancock, M.L.6    Chan, G.C.-F.7    Pui, C.-H.8    Grosveld, G.9    Downing, J.R.10


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.