Callea, Michele, Unit of Dentistry, Bambino Ges í¹ Children”™s Hospital - IRCCS, Rome, Italy, Italia

• Investigación Clínica Vol. 58 Núm. 1 - Reporte de Caso
  A c.3037G>A mutation in FBN1 gene causing Marfan syndrome with an atypically severe phenotype.
  Resumen  PDF