Fluorescence in situ hybridization analysis of t(3;12)(q26;p13): A recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromes

Blood

Volumn 88, Issue 2, 1996, Pages 682-689

  Raynaud, S D ^a   Baens, M ^b   Grosgeorge, J ^b   Rodgers, K ^b   Reid, C D L ^b   Dainton, M ^b   Dyer, M ^b   Fuzibet, J G ^b   Gratecos, N ^b   Taillan, B ^b   Ayraud, N ^b   Marynen, P ^b  

^a CNRS   (France)

^b NONE

Author keywords

[No Author keywords available]

Indexed keywords

ARTICLE; CHROMOSOME 12P; CHROMOSOME 3Q; CHROMOSOME BREAKAGE; CHROMOSOME TRANSLOCATION 12; CHROMOSOME TRANSLOCATION 3; CHRONIC MYELOID LEUKEMIA; GENE REARRANGEMENT; GENE TRANSLOCATION; HUMAN; HUMAN TISSUE; MYELODYSPLASTIC SYNDROME; PRIORITY JOURNAL;

EID: 8944246791     PISSN: 00064971     EISSN: None     Source Type: Journal    
DOI: 10.1182/blood.v88.2.682.bloodjournal882682     Document Type: Article

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