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767 Trisomies 9 and 8 detected by fluorescence in situ hybridisation in patients with systemic mastocytosis

✍ Scribed by CONFINOCOHEN, R; LISHNER, M; GOLDBERG, A; FEIGIN, M; AMIEL, A; MEKORI, Y


Book ID
119496090
Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
106 KB
Volume
97
Category
Article
ISSN
1097-6825

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## Abstract Mastocytosis is a rare disease characterized by proliferation of mast cells in one or several organs. With conventional cytogenetics about 35% of the patients have chromosomally abnormal clones in bone marrow cells. It has been proposed to include the mast cell disease among the myelopr