Características clínicas y genéticas de un paciente con síndrome de Noonan y una mutación de novo en el gen MAP2K1: Reporte de caso

Translated title of the contribution: Clinical and genetic features of a Noonan syndrome with a de novo MAP2K1 mutation: A case report

Vasti Evelyn Díaz-Quiquia, Paula Heredia, Nelson Diaz-Reyes, Christoper A. Alarcon-Ruiz*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

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