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

Cite this

van der Lelij, P., Chrzanowska, K. H., Godthelp, B. C., Rooimans, M. A., Ostra, A. B., Stumm, M., ... de Winter, J. P. (2010). Warsaw Breakage Syndrome, a Cohesinopathy Associated with Mutations in the XPD Helicase Family Member DDX11/ChIR1. American journal of human genetics, 86(2), 262-266. https://doi.org/10.1016/j.ajhg.2010.01.008