Literature DB >> 2078508

Monosomy 20: a nonrandom finding in childhood acute lymphoblastic leukemia.

D R Betts1, J E Kingston, E L Dorey, B D Young, D Webb, F E Katz, B Gibbons.   

Abstract

We describe four cases of childhood acute lymphoblastic leukemia with monosomy 20 as the sole cytogenetic abnormality. These cases represent 3.4% of cytogenetically abnormal childhood ALL studied in our institute at diagnosis. The patients presented at similar age, ranging from 31 to 36 months. All four patients remain in first remission with survival time being at least 20 months from the time of diagnosis.

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Year:  1990        PMID: 2078508     DOI: 10.1002/gcc.2870020303

Source DB:  PubMed          Journal:  Genes Chromosomes Cancer        ISSN: 1045-2257            Impact factor:   5.006


  1 in total

1.  An acquired stable variant of a dicentric dic(9;20) and complex karyotype in a Syrian childhood B-acute lymphoblastic leukemia case.

Authors:  Abdulsamad Wafa; Rami A Jarjour; Abdulmunim Aljapawe; Suher ALmedania; Thomas Liehr; Joana B Melo; Isabel M Carreira; Moneeb A K Othman; Walid Al-Achkar
Journal:  Mol Cytogenet       Date:  2020-07-10       Impact factor: 2.009

  1 in total

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