Literature DB >> 1065255

Partial deletion of long arm of chromosome 17: a specific abnormality in acute promyelocytic leukemia?

H M Golomb, J Rowley, J Vardiman, J Baron, G Locker, S Krasnow.   

Abstract

Two patients with acute promyelocytic leukemia had an identical chromosomal abnormality detected by fluoresecence banding. In each case, the clinical course was rapidly fatal, and was characterized by a lack of response to chemotherapy with cytarabine and thioguanine, and was complicated by disseminated intravascular coagulation. Bone marrow cells from each patient contained 46 chromosomes; in each instance, however, one chromosome 17 had a deletion of almost one half of the proximal portion of the long arm [del(17)(q11q21 or 22)].

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Year:  1976        PMID: 1065255

Source DB:  PubMed          Journal:  Arch Intern Med        ISSN: 0003-9926


  8 in total

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4.  15/17 translocation in acute promyelocytic leukaemia.

Authors:  J M Scheres; T W Hustinx; G A de Vaan; F J Rutten
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5.  Incidence of the 15q+;17q- chromosome translocation in acute promyelocytic leukaemia (APL).

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8.  Next-generation assessment of human epidermal growth factor receptor 2 gene (ERBB2) amplification status in invasive breast carcinoma: a focus on Group 4 by use of the 2018 American Society of Clinical Oncology/College of American Pathologists HER2 testing guideline.

Authors:  Raza S Hoda; Anita S Bowman; Ahmet Zehir; Pedram Razavi; Edi Brogi; Marc Ladanyi; Maria E Arcila; Hannah Y Wen; Dara S Ross
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  8 in total

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