1MIHARA K,KIDO M,NAKAJU N,et al. Exacerba- tion of acute leukemia bearing isolated i(17@ along with proliferation of blasts with high BMI-1 expres- sion[J]. Rinsho Ketsueki, 2007,48 : 659-- 663.
2NISHIDA H, UENO H, PARK J W, et al. Isochromo- some i(17q) as a sole cytogenetic abnormality in a case of leukemic transformation from myelodysplastic syndrome (MDS)/myeloproliferative diseases (MPD) [J]. Leuk Res,2008,32:1325--1327.
3POZDNYAKOVA O, MIRON PM, TANG G, et al. Cytogenetic abnormalities in a series of 1,029 patients with primary myelodysplastic syndromes: a report from the US with a focus on some undefined single chromosomal abnormalities [J].Cancer, 2008, 113 : 3331--3340.
4KANAGAL-SHAMANNA R,BUESO-RAMOS C E, BARKOH B, et al. Myeloid neoplasms with isolated isochromosome 17q represent a clinicopathologic enti-ty associated with myelodysplastic/myeloproliferative features,a high risk of leukemic transformation, and wild-type TP53[J].Cancer, 2012,118 : 2879-- 2888.
5KIM M J,CHO S Y,KIM M H,et al. FISH negative cryptic PML-RARA rearrangement detected by long- distance polymerase chain reaction and sequencing an- alyses:a case study and review of the literature[J]. Cancer Genet Cytogenet, 2010,203 : 278 -- 283.
6PARK T S,KIM J S,SONG J,et al. Acute promyelo cytic leukemia with insertion of PML exon 7a and par- tial deletion of exon 3 of RARA:a novel variant tran- script related to aggressive course and not detected with real-time polymerase chain reaction analysis[J]. Cancer Genet Cytogenet, 2009,188 : 103 -- 107.
7GRIMWADE D, BIONDI A, MOZZICONACCI M J, et al. Characterization of acute promyeloeytic leukemia cases lacking the classic t ( 15 ; 17) : results of the Euro- pean Working Party. Groupe Francais de Cytogenfitique Hematologique,Groupe de Fran? ais d' Hematologic Cellulaire, UK Cancer Cytogenetics Group and BIOMED 1 European Community-Concert- ed Action " Molecular Cytogenetic Diagnosis in Haematological Malignancies "[J]. Blood, 2000, 96: 1297--1308.
