Molecular analysis of cancer genomes in children with Lynch syndrome: Exploring causal associations
Dilys Weijers(Princess Máxima Center), Roland P. Kuiper(Princess Máxima Center), Steffen Hirsch(Heidelberg University), Marjolijn C.J. Jongmans(Utrecht University), Nienke van Engelen(Princess Máxima Center), Robert J. Autry(St. Jude Children's Research Hospital), Mariëtte E.G. Kranendonk(Princess Máxima Center), Jan Loeffen(Radboud University Nijmegen), Evelien de Vos‐Kerkhof(Princess Máxima Center), Jette J. Bakhuizen(Heidelberg University), Lennart Kester(Royal Netherlands Academy of Arts and Sciences), Kristian W. Pajtler(German Cancer Research Center), Natalie Jäger(German Cancer Research Center), Laura S. Hiemcke‐Jiwa(Princess Máxima Center)
Cited by 8
Related Papers
Signatures of mutational processes in human cancer
|Nature|2013|10.1k
The whole-genome landscape of medulloblastoma subtypes
|Nature|2017|1.2k