Loss at 12p detected by comparative genomic hybridization (CGH): Association with TEL-AML1 fusion and favorable prognostic features in childhood acute lymphoblastic leukemia (ALL). A multi-institutional study

J Kanerva, T Niini, K Vettenranta, P Riikonen, A Makipernaa, R Karhu, S Knuutila, UM Saarinen-Pihkala

Research output: Contribution to journalArticleScientificpeer-review

Original languageEnglish
JournalPediatric Blood & Cancer
Volume37
Issue number5
Pages (from-to)419-425
Number of pages7
ISSN0098-1532
DOIs
Publication statusPublished - Nov 2001
MoE publication typeA1 Journal article-refereed

Fields of Science

  • comparative genomic hybridization
  • acute lymphoblastic leukemia
  • TEL-AML1
  • 12p deletion
  • childhood cancer
  • TEL/AML1 FUSION
  • CHROMOSOMAL-ABNORMALITIES
  • SHORT ARM
  • DELETION
  • TEL
  • CYTOGENETICS
  • MORPHOLOGY
  • T(12-21)
  • CHILDREN
  • DISTINCT
  • 3123 Gynaecology and paediatrics
  • 3122 Cancers

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