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1 Ergebnisse
1
Low mutation burden and frequent loss of CDKN2A/B and SMARC..:
Pemov, Alexander
;
Hansen, Nancy F
;
Sindiri, Sivasish
...
Neuro-Oncology. 21 (2019) 8 - p. 981-992 , 2019
Link:
https://doi.org/10.1093/neuonc/noz028
RT Journal T1
Low mutation burden and frequent loss of CDKN2A/B and SMARCA2, but not PRC2, define premalignant neurofibromatosis type 1–associated atypical neurofibromas
UL https://suche.suub.uni-bremen.de/peid=cr-10.1093_neuonc_noz028&Exemplar=1&LAN=DE A1 Pemov, Alexander A1 Hansen, Nancy F A1 Sindiri, Sivasish A1 Patidar, Rajesh A1 Higham, Christine S A1 Dombi, Eva A1 Miettinen, Markku M A1 Fetsch, Patricia A1 Brems, Hilde A1 Chandrasekharappa, Settara C A1 Jones, Kristine A1 Zhu, Bin A1 Wei, Jun S A1 Mullikin, James C A1 Wallace, Margaret R A1 Khan, Javed A1 Legius, Eric A1 Widemann, Brigitte C A1 Stewart, Douglas R A1 National Intramural Sequencing Center (NISC) Comparative Sequencing Program A1 National Cancer Institute (NCI) Division of Cancer Epidemiology and Genetics (DCEG) Cancer Genomics Research Laboratory PB Oxford University Press (OUP) YR 2019 SN 1522-8517 SN 1523-5866 JF Neuro-Oncology VO 21 IS 8 SP 981 OP 992 LK http://dx.doi.org/https://doi.org/10.1093/neuonc/noz028 DO https://doi.org/10.1093/neuonc/noz028 SF ELIB - SuUB Bremen
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