WordNet

chrosomal abnormality in which there is one more than the normal number of chromosomes in a cell

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1. 先天性の細胞遺伝学的異常 congenital cytogenetic abnormalities
2. 骨髄異形成症候群における細胞遺伝学および分子遺伝学 cytogenetics and molecular genetics of myelodysplastic syndromes
3. 急性骨髄性白血病における細胞遺伝学 cytogenetics in acute myeloid leukemia
4. デスモイド腫瘍：疫学、危険因子、分子学的病因、臨床症状、診断、および局所療法 desmoid tumors epidemiology risk factors molecular pathogenesis clinical presentation diagnosis and local therapy
5. 肝脾T細胞性リンパ腫の臨床症状、病理学的特徴、および診断 clinical manifestations pathologic features and diagnosis of hepatosplenic t cell lymphoma

Zhang YR1, Qi JY, Liu HM, Liu W, Huang WY, Deng SH, Yi SH, Xu Y, Li ZJ, Fu MW, Zou DH, Zhao YZ, Qiu LG.
Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi.Zhonghua Xue Ye Xue Za Zhi.2013 Oct;34(10):839-43. doi: 10.3760/cma.j.issn.0253-2727.2013.10.004.
OBJECTIVE: To investigate the clinical and laboratory characteristics and survival of Chinese patients with T- cell prolymphocytic leukemia (T-PLL).METHODS: Eleven patients with T-PLL admitted in our hospital from Jan 2006 to Oct 2012 were retrospectively analyzed.RESULTS: Of the 11 patients, nine w
PMID 24171956

Clinical and cytogenetic features of a patient with partial trisomy 8q and partial monosomy 13q delineated by array comparative genomic hybridization.

Sohn YB1, Yun JN, Park SJ, Park MS, Kim SH, Lee JH.
Annals of clinical and laboratory science.Ann Clin Lab Sci.2013 Summer;43(3):332-6.
Partial trisomy 8q is rare and has distinctive clinical features, including severe mental retardation, growth impairment, dysmorphic facial appearances, cleft palate, congenital heart disease, and urogenital anomalies. Partial monosomy 13q is a rare genetic disorder displaying a variety of phenotypi
PMID 23884231

Analysis of genomic alterations on urological malignancies by fluorescence in situ hybridization

Matsuyama Hideyasu,Pan Yi,Oba Kazuo,Tsukamoto Manabu,Nagao Kazuhiro,Yamaguchi Shiro,Fukunaga Koji,Matsuda Kenji,Yoshihiro Satoru,Li Chunde,Kudren David,Bergerheim Ulf S. R.,Ekman Peter,Naito Katsusuke
The bulletin of the Yamaguchi Medical School 50(1-4), 11-18, 2003-12
… The following results had been obtained and published in the literature: Bradder cancer: Numericalalterations on chromosome 7, 9, and 17 by dual-color fruorescence in situ hybridization (FISH) demonstrated that chromosome 7 trisomy and 9 monosomy were the most frequently occurred not only in the tumor, but also in the surrounding intact bladder mucosa, and that 9 monosomy detected by using negative cytology specimen could predict early recurrence of superficial bladder cancer. …
NAID 120000864659

Trisomy/Tetrasomy of chromosome 8 and +i(8q) as the sole chromosome abnormality in three adult patients with myelomonocytic leukemia