T. Kleefstra, W. A. van Zelst-Stams, W. M. Nillesen, V. Cormier-Daire, G. Houge, N. Foulds, M. van Dooren, M. H. Willemsen, R. Pfundt, A. Turner, M. Wilson, J. McGaughran, A. Rauch, M. Zenker, M. P. Adam, M. Innes, C. Davies, A. G. López, R. Casalone, A. Weber, L. A. Brueton, A. D. Navarro, M. P. Bralo, H. Venselaar, S. P. Stegmann, H. G. Yntema, H. van Bokhoven, H. G. Brunner: Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype. In: Journal of medical genetics. Bd. 46, Nr. 9, September 2009, S. 598–606, doi:10.1136/jmg.2008.062950, PMID 19264732.
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T. Kleefstra, W. A. van Zelst-Stams, W. M. Nillesen, V. Cormier-Daire, G. Houge, N. Foulds, M. van Dooren, M. H. Willemsen, R. Pfundt, A. Turner, M. Wilson, J. McGaughran, A. Rauch, M. Zenker, M. P. Adam, M. Innes, C. Davies, A. G. López, R. Casalone, A. Weber, L. A. Brueton, A. D. Navarro, M. P. Bralo, H. Venselaar, S. P. Stegmann, H. G. Yntema, H. van Bokhoven, H. G. Brunner: Further clinical and molecular delineation of the 9q subtelomeric deletion syndrome supports a major contribution of EHMT1 haploinsufficiency to the core phenotype. In: Journal of medical genetics. Bd. 46, Nr. 9, September 2009, S. 598–606, doi:10.1136/jmg.2008.062950, PMID 19264732.
