Geerts‐Haages, A., Bossuyt, S. N. V., den Besten, I., Bruggenwirth, H., van der Burgt, I., Yntema, H. G., . . . Valstar, M. (2020). A novel UBE3A sequence variant identified in eight related individuals with neurodevelopmental delay, results in a phenotype which does not match the clinical criteria of Angelman syndrome. Mol Genet Genomic Med.
Citação norma ChicagoGeerts‐Haages, Amber, et al. "A Novel UBE3A Sequence Variant Identified in Eight Related Individuals With Neurodevelopmental Delay, Results in a Phenotype Which Does Not Match the Clinical Criteria of Angelman Syndrome." Mol Genet Genomic Med 2020.
Citação norma MLAGeerts‐Haages, Amber, et al. "A Novel UBE3A Sequence Variant Identified in Eight Related Individuals With Neurodevelopmental Delay, Results in a Phenotype Which Does Not Match the Clinical Criteria of Angelman Syndrome." Mol Genet Genomic Med 2020.