Masson, J., Demily, C., Chatron, N., Labalme, A., Rollat-Farnier, P., Schluth-Bolard, C., . . . Rossi, M. (2019). Molecular investigation, using chromosomal microarray and whole exome sequencing, of six patients affected by Williams Beuren syndrome and Autism Spectrum Disorder. Orphanet J Rare Dis.
Citación estilo ChicagoMasson, Julie, et al. "Molecular Investigation, Using Chromosomal Microarray and Whole Exome Sequencing, of Six Patients Affected By Williams Beuren Syndrome and Autism Spectrum Disorder." Orphanet J Rare Dis 2019.
Cita MLAMasson, Julie, et al. "Molecular Investigation, Using Chromosomal Microarray and Whole Exome Sequencing, of Six Patients Affected By Williams Beuren Syndrome and Autism Spectrum Disorder." Orphanet J Rare Dis 2019.