Romani, M., Micalizzi, A., Kraoua, I., Dotti, M. T., Cavallin, M., Sztriha, L., . . . Valente, E. M. (2014). Mutations in B9D1 and MKS1 cause mild Joubert syndrome: Expanding the genetic overlap with the lethal ciliopathy Meckel syndrome. BioMed Central.
Citación estilo ChicagoRomani, Marta, et al. Mutations in B9D1 and MKS1 Cause Mild Joubert Syndrome: Expanding the Genetic Overlap With the Lethal Ciliopathy Meckel Syndrome. BioMed Central, 2014.
Cita MLARomani, Marta, et al. Mutations in B9D1 and MKS1 Cause Mild Joubert Syndrome: Expanding the Genetic Overlap With the Lethal Ciliopathy Meckel Syndrome. BioMed Central, 2014.
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