Dental developmental abnormalities in a patient with subtelomeric 7q36 deletion syndrome may confirm a novel role for the SHH gene()

por Linhares, Natália D., Svartman, Marta, Salgado, Mauro Ivan, Rodrigues, Tatiane C., da Costa, Silvia S., Rosenberg, Carla, Valadares, Eugênia R.
Publicado 2013