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Corrigendum: Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification (vol 72, pg 122, 2007)

机译：更正：通过DNA测序，Southern印迹分析和多重连接依赖探针扩增鉴定的经典和非典型性冯·希佩尔·林道疾病中冯·希佩尔·林道种系突变的频率（第72卷，第122页，2007年）

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Hes F. J.; van der Luijt R. B.; Janssen A. L. W.; Zewald R. A.; de Jong G. J.; Lenders J. W.; Links T. P.; Luyten G. P. M.; Sijmons R. H.; Eussen H. J.; Halley D. J. J.; Lips C. J. M.; Pearson P. L.; van den Ouweland A. M. W.; Majoor-Krakauer D. F.;
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1. Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification. [J] . Hes F, van-der-Luijt R, Janssen A, Clinical Genetics: An International Journal of Genetics in Medicine . 2007,第2期

机译：通过DNA测序，Southern印迹分析和多重连接依赖性探针扩增鉴定经典和非典型性冯·希佩尔·林道疾病中冯·希佩尔·林道种系突变的频率。
2. Multiplex Ligation-dependent Probe Amplification Analysis Subsequent to Direct DNA Full Sequencing for Identifying ATP7B Mutations and Phenotype Correlations in Children with Wilson Disease [J] . Shim Jung Ok, Yang Hye Ran, Moon Jin Soo, Journal of Korean medical science. . 2018,第26期

机译：直接DNA全序列测序后的多重结扎依赖性探针扩增分析可用于识别威尔逊病患儿的ATP7B突变和表型相关性
3. Identification of Cyclin D1 and OtherNovel Targets for the von Hippel-Lindau Tumor Suppressor Gene by Expression Array Analysis and Investigation of Cyclin D1 Genotype as a Modifier in von Hippel-Lindau Disease (vol 62, pg 3803, 2002) [J] . Zatyka M., da Silva N. F., Clifford S. C., Cancer research: The official organ of the American Association for Cancer Research, Inc . 2015,第18期

机译：通过表达阵列分析鉴定von Hippel-Lindau肿瘤抑制基因的Cyclin D1和其他新颖靶标，并研究von Hippel-Lindau疾病的Cyclin D1基因型作为修饰因子（第62卷，第3803页，2002）
4. Multiplex Ligation-dependent Probe Amplification Analysis Subsequent to Direct DNA Full Sequencing for Identifying ATP7B Mutations and Phenotype Correlations in Children with Wilson Disease [O] . Jung Ok Shim, Hye Ran Yang, Jin Soo Moon, 2018

机译：直接全DNA测序后多重连接依赖探针扩增分析以鉴定威尔逊病患儿的ATP7B突变和表型相关性。
5. Germline mutations in the von Hippel-Lindau (VHL) gene in patients from Poland: disease presentation in patients with deletions of the entire VHL gene [O] . Cybulski, C, Krzystolik, K, Murgia, A, 2002

机译：波兰患者的von Hippel-Lindau（VHL）基因中的种系突变：缺失整个VHL基因的患者的疾病表现

Corrigendum: Frequency of Von Hippel-Lindau germline mutations in classic and non-classic Von Hippel-Lindau disease identified by DNA sequencing, Southern blot analysis and multiplex ligation-dependent probe amplification (vol 72, pg 122, 2007)

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