Ropers, Hans-Hilger Dept. of Human Molecular Genetics (Head: Hans-Hilger Ropers), Max Planck Institute for Molecular Genetics, Max Planck Society;
Engenheiro, E., Saraiva, J., Carreira, I., Ramos, L., Ropers, H.-H., Silva, E., et al. (2007). Cytogenetically invisible microdeletions involving PITX2 in Rieger syndrome. Clinical Genetics: an International Journal of Genetics in Medicine, 72(5), 464-470. doi:10.1111/j.1399-0004.2007.00879.x.