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Targeted genomic enrichment and massively parallel sequencing identifies novel nonsyndromic hearing impairment pathogenic variants in Cameroonian families

机译：靶向基因组富集和大规模平行测序识别喀麦隆家族中的新型非合成性听力损伤致病性变异

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K. Lebeko; C. M. Sloan-Heggen; J. J. N. Noubiap; C. Dandara; D. L. Kolbe; S. S. Ephraim; K. T. Booth; H. Azaiez; R. L. P. Santos-Cortez; S. M. Leal; R. J. H. Smith; A. Wonkam;
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1. Targeted genomic enrichment and massively parallel sequencing identifies novel nonsyndromic hearing impairment pathogenic variants in Cameroonian families [J] . Lebeko K., Sloan-Heggen C. M., Noubiap J. J. N., Clinical Genetics: An International Journal of Genetics in Medicine . 2016,第3期

机译：靶向基因组富集和大规模平行测序可确定喀麦隆家庭中新型的非综合征性听力障碍致病变异
2. Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss [J] . Qinjun Wei, Hongmei Zhu, Xuli Qian, Journal of Translational Medicine . 2014,第1期

机译：靶向基因组捕获和大规模平行测序，以鉴定导致中国遗传性听力损失的新变异
3. Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families [J] . Zippora Brownstein, ?Lilach M Friedman, ?Hashem Shahin, Genome Biology . 2011,第9期

机译：靶向基因组捕获和大规模平行测序，以鉴定中东家庭遗传性听力损失的基因
4. Targeted profiling of 5-(hydroxy)methylcytosine in genomic DNA from human livers: Next-generation sequencing of target enriched DNA reveals unexpectedly high interindividual variability of cytosine methylation and hydroxymethylation [C] . Ivanov Maxim, Ingelman-Sundberg Magnus, Kals Mart, IEEE International Conference on Bioinformatics and Biomedicine . 2014

机译：人类肝脏基因组DNA中5-（羟）甲基胞嘧啶的靶向分析：富含靶DNA的下一代测序揭示了胞嘧啶甲基化和羟甲基化的意料之外的高度个体差异
5. Molecular characterization and clinical implementation of breast cancer genomics using massive parallel sequencing and microarray. [D] . Zhao, Wei. 2014

机译：使用大规模平行测序和微阵列的乳腺癌基因组学的分子表征和临床实施。
6. Targeted genomic enrichment and massively parallel sequencing identifies novel nonsyndromic hearing impairment pathogenic variants in Cameroonian families [O] . K. Lebeko, C. M. Sloan-Heggen, J. J. N. Noubiap, -1

机译：靶向基因组富集和大规模平行测序可确定喀麦隆家庭中新型的非综合征性听力障碍致病变异
7. Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss [O] . 2014

机译：靶向基因组捕获和大规模平行测序，以鉴定引起中国遗传性听力损失的新变异
8. Tumor Genomic Profiling in Breast Cancer Patients Using Targeted Massively Parallel Sequencing. [R] . Wagle, N. 2016

机译：基于靶向大规模平行测序的乳腺癌患者肿瘤基因组谱分析。

Targeted genomic enrichment and massively parallel sequencing identifies novel nonsyndromic hearing impairment pathogenic variants in Cameroonian families

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