Díaz-Quiquia, V. E., Heredia, P., Diaz-Reyes, N., & Alarcon-Ruiz, C. A. (2022). Clinical and genetic features of a Noonan syndrome with a de novo MAP2K1 mutation: A case report.
Citación estilo ChicagoDíaz-Quiquia, Vasti Evelyn, Paula Heredia, Nelson Diaz-Reyes, y Christoper A. Alarcon-Ruiz. Clinical and Genetic Features of a Noonan Syndrome With a De Novo MAP2K1 Mutation: A Case Report. 2022.
Cita MLADíaz-Quiquia, Vasti Evelyn, Paula Heredia, Nelson Diaz-Reyes, y Christoper A. Alarcon-Ruiz. Clinical and Genetic Features of a Noonan Syndrome With a De Novo MAP2K1 Mutation: A Case Report. 2022.
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