Acute lymphocytic leukemia with 9p anomalies: A report of four additional cases and review of the literature
Childhood acute lymphocytic leukemia (ALL) with partial deletion of the short arm of chromosome 9 (9p−), particularly in the p21–22 region, associated with bulky disease, has been regarded as a possible subgroup of ALL. We have reviewed clinical and cytologic data in 128 cases of ALL (childhood and...
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Veröffentlicht in: | Cancer genetics and cytogenetics 1988-07, Vol.33 (1), p.99-109 |
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