The MTG proteins: chromatin repression players with a passion for networkingROSSETTI, Stefano; HOOGEVEEN, André T; SACCHI, Nicoletta et al.Genomics (San Diego, Calif.). 2004, Vol 84, Num 1, pp 1-9, issn 0888-7543, 9 p.Article

Knockout mouse model for Fxr2: a model for mental retardationBONTEKOE, Carola J. M; MCILWAIN, Kellie L; NGAN CHING CHENG et al.Human molecular genetics (Print). 2002, Vol 11, Num 5, pp 487-498, issn 0964-6906Article

Reduced Telomere Length in Individuals with FMR1 Premutations and Full MutationsJENKINS, Edmund C; TASSONE, Flora; LINGLING YE et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 5, pp 1060-1065, issn 1552-4825, 6 p.Article

Fragile X syndrome : An epigenetic diseaseSTOYANOVA, Violeta; HOOGEVEEN, André T.The molecular basis of fragile X syndrome. 2005, pp 1-16, isbn 81-7736-257-7, 1Vol, 16 p.Book Chapter

Myeloid maturation block by AML1-MTG16 is associated with Csf1r epigenetic downregulationROSSETTI, Stefano; VAN UNEN, Leontine; TOUW, Ivo P et al.Oncogene (Basingstoke). 2005, Vol 24, Num 34, pp 5325-5332, issn 0950-9232, 8 p.Article

Fxr1 knockout mice show a striated muscle phenotype: implications for Fxr1p function in vivoMIENTJES, Edwin J; WILLEMSEN, Rob; NELSON, David L et al.Human molecular genetics (Print). 2004, Vol 13, Num 13, pp 1291-1302, issn 0964-6906, 12 p.Article

The FMR1 CGG repeat mouse displays ubiquitin-positive intranuclear neuronal inclusions; implications for the cerebellar tremor/ataxia syndromeWILLEMSEN, Rob; HOOGEVEEN-WESTERVELD, Marianne; HAGERMAN, Paul J et al.Human molecular genetics (Print). 2003, Vol 12, Num 9, pp 949-959, issn 0964-6906, 11 p.Article

The transcriptional corepressor MTG16a contains a novel nucleolar targeting sequence deranged in t (16; 21)-positive myeloid malignanciesHOOGEVEEN, André T; ROSSETTI, Stefano; STOYANOVA, Violeta et al.Oncogene (Basingstoke). 2002, Vol 21, Num 43, pp 6703-6712, issn 0950-9232, 10 p.Article