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A new variant translocation 11;17 in a patient with acute promyelocytic leukemia together with t(7;12).

作者信息

Najfeld V, Scalise A, Troy K

机构信息

Polly Annenberg Levee Hematology Center, Mount Sinai Medical Center, New York, NY 10029.

出版信息

Cancer Genet Cytogenet. 1989 Nov;43(1):103-8. doi: 10.1016/0165-4608(89)90133-7.

DOI:10.1016/0165-4608(89)90133-7
PMID:2790765
Abstract

Bone marrow cells from the majority of patients with acute promyelocytic leukemia (APL) are characterized by t(15;17)(q22;q11-12). At least 12 variant translocations have both also reported, and in each case, either abnormal chromosome 15 or del(17q) or both were involved in complex rearrangements. We report a patient with APL showing two translocations without apparent involvement of chromosome 15 and without del(17q). The karyotype was 46,XY,t(7;12)(p15;p13),t(11;17)(q13;q12). Rearrangement involving t(11;17) is probably associated with APL, while t(7;12) appears to be therapy related.

摘要

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2
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Cryptic t(15;17) acute promyelocytic leukemia with a karyotype of add(11)(p15) and t(13,20)- A case report with a literature review.隐匿性 t(15;17)急性早幼粒细胞白血病伴附加异常 11(p15)和 t(13,20)——附文献复习的 1 例报告
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Rearrangements of the retinoic acid receptor alpha and promyelocytic leukemia zinc finger genes resulting from t(11;17)(q23;q21) in a patient with acute promyelocytic leukemia.
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