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Nature Communications|January 17, 2018
Elucidating the genomic architecture of Asian EGFR-mutant lung adenocarcinoma through multi-region exome sequencingRahul Nahar, Weiwei Zhai, Tong Zhang, et al.
Plos One|March 8, 2014
Detection of chromosomal breakpoints in patients with developmental delay and speech disordersKagistia H Utami, Axel M Hillmer, Irene Aksoy, et al.
Genome Biology|December 15, 2012
Whole-genome reconstruction and mutational signatures in gastric cancerNiranjan Nagarajan, Denis Bertrand, Axel M Hillmer, et al.
Cell Reports|July 7, 2015
Recurrent Fusion Genes in Gastric Cancer: CLDN18-ARHGAP26 Induces Loss of Epithelial IntegrityFei Yao, Jaya P Kausalya, Yee Yen Sia, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 15, 2021
Integrative Profiling of T790M-Negative EGFR-Mutated NSCLC Reveals Pervasive Lineage Transition and Therapeutic OpportunitiesKhi Pin Chua, Yvonne H F Teng, Aaron C Tan, et al.
Nature Genetics|January 10, 2017
De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal developmentChristopher T Gordon, Shifeng Xue, Gökhan Yigit, et al.
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