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Search Results - David S. Cram
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Cruxome: a powerful tool for annotating, interpreting and reporting genetic variants by Qingmei Han, Ying Yang, Shengyang Wu, Yingchun Liao, Shuang Zhang, Hongbin Liang, David S. Cram, Yu Zhang
Published 2021-06-01
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Cell-free DNA test for pathogenic copy number variations: A retrospective study by Hong-Lei Duan, Jie Li, Wan-Jun Wang, David S. Cram, Wei Liu, Pei-Xuan Cao, Xiang-Yu Zhu, Ya-Li Hu
Published 2021-11-01
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Characterisation Of Forebrain Neurons Derived From Late-Onset Huntington’s Disease Human Embryonic Stem Cell Lines by Jonathan Christos Niclis, Jonathan Christos Niclis, Anita ePinar, John M Haynes, Walaa eAlsanie, Robert eJenny, Mirella eDottori, David S Cram
Published 2013-04-01
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REDBot: Natural language process methods for clinical copy number variation reporting in prenatal and products of conception diagnosis by Mengmeng Liu, Yunshan Zhong, Hongqian Liu, Desheng Liang, Erhong Liu, Yu Zhang, Feng Tian, Qiaowei Liang, David S. Cram, Hua Wang, Lingqian Wu, Fuli Yu
Published 2020-11-01
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A comprehensive multiplex PCR based exome-sequencing assay for rapid bloodspot confirmation of inborn errors of metabolism by Wenjie Wang, Jianping Yang, Jinjie Xue, Wenjuan Mu, Xiaogang Zhang, Wang Wu, Mengnan Xu, Yuyan Gong, Yiqian Liu, Yu Zhang, Xiaobing Xie, Weiyue Gu, Jigeng Bai, David S. Cram
Published 2019-01-01
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Genetic profiling of primary and secondary tumors from patients with lung adenocarcinoma and bone metastases reveals targeted therapy options by Long Huang, Xiao-Liu Jiang, Hong-Bin Liang, Jian-Cheng Li, Li-Han Chin, Jian-Ping Wei, Rui-Ru Wang, Jing Cai, Qiang Xiong, Lien-Tu Wang, David S. Cram, An-Wen Liu
Published 2020-09-01
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