Ropers, Hans-Hilger Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;
Poirier, K., Francis, F., Hamel, B., Moraine, C., Fryns, J. P., Ropers, H.-H., et al. (2005). Mutations in exon 1 of MECP2B are not a common cause of X-linked mental retardation in males. Druckausgaben (und Verfilmungen), 13(5), 523-524. doi:10.1038/sj.ejhg.5201399.
