TEL gene is involved in myelodysplastic syndromes with either the typical t(5;12)(q33;p13) translocation or its variant t(10;12)(q24;p13)

Blood

Volumn 85, Issue 10, 1995, Pages 2848-2852

  Wlodarska, I ^b   Mecucci, C ^b   Marynen, P ^b   Guo, C ^b   Franckx, D ^b   La Starza, R ^b   Aventin, A ^b   Bosly, A ^b   Martelli, M F ^b   Cassiman, J J ^b   Van Den Berghe, H ^a  

^a CENTER FOR HUMAN GENETICS   (Belgium)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CARCINOGENESIS; CASE REPORT; CHROMOSOME 12; CHROMOSOME TRANSLOCATION 10; CHROMOSOME TRANSLOCATION 5; CHRONIC MYELOID LEUKEMIA; CLINICAL FEATURE; DNA PROBE; EOSINOPHILIA; FLUORESCENCE IN SITU HYBRIDIZATION; GENE FUSION; GENE LOCATION; GENETIC VARIABILITY; HUMAN; MOLECULAR CLONING; MONOCYTOSIS; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL;

EID: 0029033747     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v85.10.2848.bloodjournal85102848     Document Type: Article

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