i (17) (q10) was a significant independent negative prognostic factor. Infant medulloblastomas may be a distinct genetic subset from those of older patients. 展开 关键词: Medulloblastoma comparative genomic hybridization isochromosome 17q primitive neuroectodermal tumor unsupervised cluster analysis SAM DOI...
1) Isochromosome 17q 染色体易位i(17q-)2) chromosome translocation 染色体易位 1. Chromosome translocations in Chinese medical X-ray workers analyzed by fluorescence in situ hybridization; 荧光原位杂交法分析中国医用诊断X射线工作者的染色体易位畸变 2. Chromosome translocations were analyzed by chromosome...
Isolated isochromosome 17q: a distinct type of mixed myeloproliferative disorder/myelodysplastic syndrome with an aggressive clinica... The Breakpoint Region of the Most Common Isochromosome, i(17q), in Human Neoplasia Is Characterized by a Complex Genomic Architectur... ...
i(18q) was found in cultured amniotic cells. Fetal blood sampling confirmed the presence of both cell lines. The pregnancy was terminated and the two cell lines were demonstrated in varyi... SD Sutton,MA Ridler - 《Journal of Medical Genetics》 被引量: 36发表: 1986年 Isochromosome (17q)...
Isochromosome 17q in two cases of acute blast transformation in myeloproliferative disorders Two case of acute blast cell transformation in myeloproliferative disorders associated with a dicentric 17q isochromosome are reported. In both cases, the karyotypes also also included a Philadelphia 9q;22q tran...
The most common and recurrent hPSC abnormalities involve whole or partial gains on chromosomes 1, 12, 17, 20, and X (Baker et al., 2016; International Stem Cell Initiative et al., 2011; Lund et al., 2012). Strikingly, chromosome 20q aberrations have been found in almost 20% of hPSCs...
Recurrent abnormalities are del(5q), monsomy 7, del(7q), del(20q), del(17p) and del(11q).A chromosome 20q deletion is seen in about 2% of MDS cases. Patients with a sole del(20q) have a favourable outcome compared to patients with additional abnormalities such as del(5q), del...
We have shown that an i(17q) is the most frequent abnormality in central nervous system primitive neuroectodermal tumors (PNETs; medulloblastoma), implicating the presence of a tumor suppressor gene which maps to 17p. In the present study, we investigated whether the deletion of chromosome arm...
Trisomy 18 caused by isochromosome 18p and 18q formation: Is there a milder phenotype? 来自 Wiley 喜欢 0 阅读量: 42 作者:GM Maruotti,F Fabbrini,R Napolitano,R Genesio,A Conti,GM Milanes,LL Mazzarelli,P Martinelli 摘要: No abstract is available for this article.关键词:...