Noonan syndrome: Severe phenotype and PTPN11 mutations

Salas, PC; Gomez-Molina, G; Carreto-Alba, P; Granell-Escobar, R; Vazquez-Rico, I; Leon-Justel, A

Salas, PC (reprint author), Juan Ramon Jimenez Hosp, Human Genet Unit, Huelva, Spain.

MEDICINA CLINICA, 2019; 152 (2): 62

Abstract

Introduction and objective: Noonan syndrome (NS) is a genetic disorder characterized by a wide range of distinctive features and health problems. It c......

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