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Homozygous deletion of TNFRSF4, TP73, PPAP2B and DPYD at 1p and PDCD5 at 19q identified by multiplex ligation-dependent probe amplification (MLPA) analysis in pediatric anaplastic glioma with questionable oligodendroglial component

机译：儿科间变性神经胶质瘤伴有少突胶质细胞成分的多重连接依赖探针扩增（MLPA）分析鉴定出1p处TNFRSF4，TP73，PPAP2B和DPYD在1p和PDCD5的纯合缺失

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Miguel Torres-Martín; Carolina Peña-Granero; Fernando Carceller; Manuel Gutiérrez; Rommel R Burbano; Giovanny R Pinto; Javier S Castresana; Bárbara Melendez; Juan A Rey;
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1. Homozygous deletion of TNFRSF4, TP73, PPAP2B and DPYD at 1p and PDCD5 at 19q identified by multiplex ligation-dependent probe amplification (MLPA) analysis in pediatric anaplastic glioma with questionable oligodendroglial compon [J] . Miguel Torres-Martín, Carolina Pe?a-Granero, Fernando Carceller, Molecular cytogenetics . 2014,第1期

机译：小儿间变性神经胶质瘤伴可疑少突胶质胶质瘤的多重结扎依赖性探针扩增（MLPA）分析鉴定出1p处TNFRSF4，TP73，PPAP2B和DPYD在1p和PDCD5的纯合缺失
2. Multiplex ligation-dependent probe amplification for the detection of 1p and 19q chromosomal loss in oligodendroglial tumors. [J] . Natte R, van Eijk R, Eilers P, Brain pathology . 2005,第3期

机译：多重连接依赖探针扩增可检测少突胶质细胞瘤中的1p和19q染色体缺失。
3. Allelic status of 1p and 19q in oligodendrogliomas and glioblastomas: multiplex ligation-dependent probe amplification versus loss of heterozygosity. [J] . Franco Hernandez C, Martinez Glez V, de Campos JM Cancer genetics and cytogenetics . 2009,第2期

机译：少突胶质细胞瘤和胶质母细胞瘤中1p和19q的等位基因状态：多重连接依赖性探针扩增与杂合性丧失。
4. Homozygous deletion of TNFRSF4 TP73 PPAP2B and DPYD at 1p and PDCD5 at 19q identified by multiplex ligation-dependent probe amplification (MLPA) analysis in pediatric anaplastic glioma with questionable oligodendroglial component [O] . Miguel Torres-Martín, Carolina Peña-Granero, Fernando Carceller, 2014

机译：儿科间变性神经胶质瘤伴有少突胶质成分的多重连接依赖探针扩增（MLPA）分析鉴定出1p处TNFRSF4TP73PPAP2B和DPYD在1p和PDCD5的纯合缺失
5. Cryptic intragenic deletion of the SHOX gene in a family with Léri-Weill dyschondrosteosis detected by Multiplex Ligation-Dependent Probe Amplification (MLPA) Deleção críptica intragênica do gene SHOX em uma família com discondrosteose de Léri-Weill detectada por Multiplex Ligation-Dependent Probe Amplification (MLPA) [O] . Mariana F. A. Funari, Alexander A. L. Jorge, Emilia M. Pinto, 2008

机译：通过多重连接依赖探针扩增（MLPA）检测到的莱里-威尔氏软骨异常的家庭中的SHOX基因的隐性基因内删除（MLPA） MLPA）

Homozygous deletion of TNFRSF4, TP73, PPAP2B and DPYD at 1p and PDCD5 at 19q identified by multiplex ligation-dependent probe amplification (MLPA) analysis in pediatric anaplastic glioma with questionable oligodendroglial component

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