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Escape from gene silencing in ICF syndrome: evidence for advanced replication time as a major determinant.

C. Wijmenga, M. D'Esposito, G. Gimelli, 2000, Human molecular genetics.

Reactivation of XIST in normal fibroblasts and a somatic cell hybrid: abnormal localization of XIST RNA in hybrid cells.

T. Canfield, R. Hansen, S. Gartler, 1998, Proceedings of the National Academy of Sciences of the United States of America.

The DNMT3B DNA methyltransferase gene is mutated in the ICF immunodeficiency syndrome.

C. Wijmenga, T. Canfield, R. Hansen, 1999, Proceedings of the National Academy of Sciences of the United States of America.

SMS2 deficiency impairs PKCδ-regulated B cell tolerance in the germinal center.

Christopher A. J. Roman, C. Huan, Peiqi Ou, 2021, Cell reports.