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Noonan syndrome: Severe phenotype and PTPN11 mutations

Crossref DOI link: https://doi.org/10.1016/j.medcle.2018.03.033

Published Print: 2019-01

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Carrasco Salas, Pilar

Gómez-Molina, Gertrudis

Carreto-Alba, Páxedes

Granell-Escobar, Reyes

Vázquez-Rico, Ignacio

León-Justel, Antonio
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Article Title: Noonan syndrome: Severe phenotype and PTPN11 mutations

Journal Title: Medicina Clínica (English Edition)

CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.medcle.2018.03.033

Content Type: simple-article

Copyright: © 2018 Elsevier España, S.L.U. All rights reserved.