Hodgetts Morton, V., Quinlan‐Jones, E., Butts, N., Williams, D., Hamilton, S., Marton, T., & Morris, K. (2017). The first antenatal diagnosis of KBG syndrome: A microdeletion at chromosome 16q24.2q24.3 containing multiple genes including ANKRD11 associated with the disorder. Clin Case Rep.

Hodgetts Morton, Victoria, Elizabeth Quinlan‐Jones, Natasha Butts, Denise Williams, Sue Hamilton, Tamas Marton, a Katie Morris. "The First Antenatal Diagnosis of KBG Syndrome: A Microdeletion At Chromosome 16q24.2q24.3 Containing Multiple Genes Including ANKRD11 Associated With the Disorder." Clin Case Rep 2017.

Hodgetts Morton, Victoria, et al. "The First Antenatal Diagnosis of KBG Syndrome: A Microdeletion At Chromosome 16q24.2q24.3 Containing Multiple Genes Including ANKRD11 Associated With the Disorder." Clin Case Rep 2017.