Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromes.
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P. Marynen | J. Grosgeorge | S. Raynaud | N. Ayraud | M. Baens | C. Reid | B. Taillan | N. Gratecos | M. Dyer | M. Dainton | J. Fuzibet | K. Rodgers | Sophie D. Raynaud | Martin J. S. Dyer | Martin J. S. Dyer | Noel Ayraud