Trisomy 8 detection in granulomonocytic, erythrocytic and megakaryocytic lineages by chromosomal in situ suppression hybridization in a case of refractory anaemia with ringed sideroblasts complicating the course of paroxysmal nocturnal haemoglobinuria.

Autor: PArlier, V., Tiainen, M., Beris, Ph., Miescher, P. A., Kimuutila, S., Bellomo, M. Jotterand
Zdroj: British Journal of Haematology; Jun1992, Vol. 81 Issue 2, p296-304, 9p
Databáze: Complementary Index
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