Delineation of a 6 cM commonly deleted region in childhood acute lymphoblastic leukemia on the 6q chromosomal arm (original) (raw)

Molecular Cytogenetics

Leukemia volume 11, pages 228–232 (1997)Cite this article

Abstract

Deletion of the long arm of human chromosome 6 in acute lymphoblastic leukemia (ALL) has been shown by cytogenetic studies in 4–11% of cases. To characterize further the region of deletion and to precisely establish its frequency, we studied loss of heterozygozity (LOH) in 120 children with ALL using polymorphic markers located from the 6q14-15 chromosomal band to the telomere. LOH was detected in eight patients. A single region of LOH, flanked distally by D6S1594 and proximally by D6S301 was detected. These DNA markers are separated by 6 cM and are approximately located at the 6q21-22 band. Our present results delineate a region that is likely to contain a tumor-suppressor gene involved in a subset of childhood ALLs.

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Authors and Affiliations

  1. INSERM U409, Faculté de Médecine X Bichat, Paris, France
    B Gérard & B Grandchamp
  2. Service de Biochimie Génétique and the Service d’Hématologie, Hôpital R Debré, Paris, France
    H Cavé, C Guidal, E Vilmer & B Grandchamp
  3. Hôpital Purpan, Toulouse, France
    N Dastugue

Authors

  1. B Gérard
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  2. H Cavé
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  3. C Guidal
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  4. N Dastugue
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  5. E Vilmer
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  6. B Grandchamp
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Gérard, B., Cavé, H., Guidal, C. et al. Delineation of a 6 cM commonly deleted region in childhood acute lymphoblastic leukemia on the 6q chromosomal arm.Leukemia 11, 228–232 (1997). https://doi.org/10.1038/sj.leu.2400566

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