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American Journal of Medical Genetics. Part A|May 7, 2011
Distinctive phenotype in 9 patients with deletion of chromosome 1q24-q25Deepika D'Cunha Burkardt, Jill A Rosenfeld, Maria L Helgeson, et al.American Journal of Medical Genetics. Part A|June 23, 2015
Inside the 8p23.1 duplication syndrome; eight microduplications of likely or uncertain clinical significanceJohn C K Barber, Jill A Rosenfeld, John M Graham, et al.American Journal of Human Genetics|April 30, 2013
ZC4H2 mutations are associated with arthrogryposis multiplex congenita and intellectual disability through impairment of central and peripheral synaptic plasticityHiromi Hirata, Indrajit Nanda, Anne van Riesen, et al.Pageof 2