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A rare mutation in a patient with Noonan syndrome with multiple lentigines

Detalles Bibliográficos
Autores principales:	Blanco-Cintrón, Manuel E., Pabón-González, Fabiola, Sánchez-Flores, Xavier
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Elsevier 2023
Materias:	Case Report
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10238803/ https://www.ncbi.nlm.nih.gov/pubmed/37274147 http://dx.doi.org/10.1016/j.jdcr.2023.04.006

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