R. R. Gomes

Rett syndrome in a boy with a 47,XXY karyotype confirmed by a rare mutation in the MECP2 gene.

M. Zatz, J. S. Schwartzman, A. Bernardino, 2001, Neuropediatrics.

Autosomal-dominant Ankyloglossia and Tooth Number Anomalies

L. M. de Paula, K. Doudney, J. Grinham, 2010, Journal of dental research.