Incidence of chromosome abnormalities and clinical significance of karyotype in de novo acute myeloid leukemia-Reference-Cited by-同舟云学术

Incidence of chromosome abnormalities and clinical significance of karyotype in de novo acute myeloid leukemia

Published:1993-05 Issue:1 Volume:67 Page:28-34
ISSN:0165-4608
Container-title:Cancer Genetics and Cytogenetics
language:en
Short-container-title:Cancer Genetics and Cytogenetics

Author:

Stasi Roberto,Del Poeta Giovanni,Masi Mario,Tribalto Maurizio,Venditti Adriano,Papa Gruseppe,Nicoletti Benedetto,Vernole Patrizia,Tedeschi Bruna,Delaroche Isabella,Mingarelli Rita,Dallapiccola Bruno

Publisher

Elsevier BV

Subject

Cancer Research,Genetics,Molecular Biology

Reference15 articles.

1. Refined chromosome study helps define prognostic subgroups in most patients with primary myelodysplastic syndrome and acute myelogenous leukemia;Yunis;Br J Haematol,1988

2. Fourth International Workshop on Chromosomes in Leukemia (FIWCL),1984

3. Prognostic significance of chromosomal abnormalities in acute nonlymphocytic leukemia: a study of 343 patients;Berger;Cancer Genet Cytogenet,1987

4. The clinical significance of karyotype in acute myelogenous leukemia;Arthur;Cancer Genet Cytogenet,1989

5. Cytogenetics and their prognostic value in de novo acute myeloid leukemia: A report on 283 cases;Fenaux;Br J Haematol,1989

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