Haaf, Thomas Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;
Lemmers, R. J. L. F., Osborn, M., Haaf, T., Rogers, M., Frants, R. R., Padberg, G. W., et al. (2003). D4F104S1 deletion in facioscapulohumeral muscular dystrophy - Phenotype, size, and detection. Neurology, 61(2), 178-183.