A case report of Noonan syndrome diagnosed in primary healthcare

Article

Abstract: Noonan syndrome is an autosomal dominant inherited disorder with variable phe-notypic expression. It

Palabras claves:

Congenital heart defects, genetic diseases, Noonan syndrome

Autores:

Alicia M. Zavala-Calahorrano, Andrea Cristina Zurita-Leal, Jenny Villaroel-Vargas, Lucía Molina-Vargas

Fuentes:

scopus