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Mitotic recombination and compound-heterozygous mutations are predominant NF1-inactivating mechanisms in children with juvenile myelomonocytic leukemia and neurofibromatosis type 1
Steinemann, D., Arning, L., Praulich, I., Stuhrmann, M., Hasle, H., Stary, J., Schlegelberger, B., Niemeyer, C. M., Flotho, C.Volume:
95
Language:
english
Journal:
Haematologica
DOI:
10.3324/haematol.2009.010355
Date:
February, 2010
File:
PDF, 143 KB
english, 2010