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Jump to: 2018 | 2011
Number of items: 2.

2018

Dentro, Stefan, Leshchiner, Ignaty, Haase, Kerstin ORCID: 0000-0002-0944-5618, Wintersinger, Jeff, Deshwar, Amit, Tarabichi, Maxime ORCID: 0000-0002-1635-2348, Rubanova, Yulia, Yu, Kaixian, Garcia, Ignacio Vazquez, Macintyre, Geoff, Kleinheinz, Kortine, Livitz, Dimitri, Malikic, Salem, Donmez, Nilgun, Sengupta, Subhajit, Ji, Yuan, Demeulemeester, Jonas, Anur, Pavana, Jolly, Clemency, Cmero, Marek, Rosebrock, Daniel, Schumacher, Steve, Fan, Yu, Fittall, Matthew, Yao, Xiaotong, Lee, Juhee, Schlesner, Matthias, Zhu, Hongtu, Adams, David, Getz, Gad, Boutros, Paul, Imielinski, Marcin, Beroukhim, Rameen, Sahinalp, Cenk, Peifer, Martin, Martincorena, Inigo, Markowetz, Florian, Mustonen, Ville, Yuan, Ke, Gerstung, Moritz, Wang, Wenyi, Spellman, Paul, Morris, Quaid, Wedge, David and Van Loo, Peter (2018). Pervasive intra-tumour heterogeneity and subclonal selection across cancer types. Cancer Res., 78 (13). PHILADELPHIA: AMER ASSOC CANCER RESEARCH. ISSN 1538-7445

2011

Pierson, Tyler Mark, Adams, David, Bonn, Florian, Martinelli, Paola, Cherukuri, Praveen F., Teer, Jamie K., Hansen, Nancy F., Cruz, Pedro, Mullikin, James C., Blakesley, Robert W., Golas, Gretchen, Kwan, Justin, Sandler, Anthony ORCID: 0000-0001-9440-2964, Fajardo, Karin Fuentes, Markello, Thomas, Tifft, Cynthia, Blackstone, Craig, Rugarli, Elena I., Langer, Thomas ORCID: 0000-0003-1250-1462, Gahl, William A. and Toro, Camilo (2011). Whole-Exome Sequencing Identifies Homozygous AFG3L2 Mutations in a Spastic Ataxia-Neuropathy Syndrome Linked to Mitochondrial m-AAA Proteases. PLoS Genet., 7 (10). SAN FRANCISCO: PUBLIC LIBRARY SCIENCE. ISSN 1553-7390

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