Noonan syndrome: Severe phenotype and PTPN11 mutations

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Medicina Clínica 2018 / 4

Noonan syndrome: Severe phenotype and PTPN11 mutations

Carrasco Salas, Pilar, Gómez-Molina, Gertrudis, Carreto-Alba, Páxedes, Granell-Escobar, Reyes, Vázquez-Rico, Ignacio, León-Justel, Antonio
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Language:
english
Journal:
Medicina Clínica
DOI:
10.1016/j.medcli.2018.03.015
Date:
April, 2018
File:
PDF, 393 KB
english, 2018
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