Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChIR1

P. van der Lelij, K.H. Chrzanowska, B.C. Godthelp, M.A. Rooimans, A.B. Ostra, M. Stumm, MZ Zdzienicka, H. Joenje, J.P. de Winter

Research output: Contribution to journalArticleAcademicpeer-review

Original languageUndefined/Unknown
Pages (from-to)262-266
JournalAmerican journal of human genetics
Volume86
Issue number2
DOIs
Publication statusPublished - 2010

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