Exome sequencing identifies recurrent somatic mutations in EIF1AX and SF3B1 in uveal melanoma with disomy 3
Nature Genetics2013Vol. 45(8), pp. 933–936
Citations Over TimeTop 1% of 2013 papers
Marcel Martin, Lars Maßhöfer, Petra Temming, Sven Rahmann, Claudia H.D. Metz, Norbert Bornfeld, Johannes van de Nes, Ludger Klein‐Hitpaß, Alan G. Hinnebusch, Bernhard Horsthemke, Dietmar Lohmann, Michael Zeschnigk
Related Papers
- → Deletion of 7p or monosomy 7 in pediatric acute lymphoblastic leukemia is an adverse prognostic factor: a report from the Children's Cancer Group(2004)67 cited
- → Familial Acute Myeloid Leukemia with Monosomy 7(2000)26 cited
- → SIGNIFICANCE OF MONOSOMY 7 IN MYELOID LEUKEMIAS IN CHILDREN(2000)2 cited
- → A Complex Translocation (5;7) in a Patient with Acute Nonlymphocytic Leukemia Evolved from a Myelodysplastic Syndrome(1998)2 cited
- → SIGNIFICANCE OF MONOSOMY 7 IN MYELOID LEUKEMIAS IN CHILDREN(2000)