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Targeted genomic capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss

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

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1. 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
2. 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
3. Novel myosin mutations for hereditary hearing loss revealed by targeted genomic capture and massively parallel sequencing [J] . BrownsteinZ., Abu-RayyanA., Karfunkel-DoronD., European journal of human genetics: EJHG . 2014,第6期

机译：通过靶向基因组捕获和大规模平行测序揭示了遗传性听力损失的新型肌球蛋白突变
4. DEFECTS IN THE ATP2B2 GENE CAUSING HEREDITARY HEARING AND BALANCE LOSS IN MICE AND HUMANS:A BIOPHYSICAL STUDY OF NORMAL AND MUTATED PMCA2 PUMP FUNCTION [C] . MARIO BORTOLOZZI NATO Advanced Study Institute on Biophotonics: Spectroscopy, Imaging, Sensing, and Manipulation . 2011

机译：ATP2B2基因的缺陷导致遗传性听力和小鼠和人类的失利：正常和突变PMCA2泵功能的生物物理研究
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 capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss [O] . Qinjun Wei, Hongmei Zhu, Xuli Qian, 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
7. Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in middle eastern families [O] . Zippora Brownstein, Lilach M Friedman, Hashem Shahin, 2011

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
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 capture and massively parallel sequencing to identify novel variants causing Chinese hereditary hearing loss

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