Genetic variants in the <i>KDM6B</i> gene are associated with neurodevelopmental delays and dysmorphic featuresElliot Stolerman, Raymond J. Louie, Kristin G. Monaghan et al.|American Journal of Medical Genetics Part A|2019Cited by 54
Fragile X syndrome phenotype with normal <i>FMR1</i> gene studiesNigel F. Clarke, Rob Willemsen, David Mowat et al.|American Journal of Medical Genetics Part A|2004Cited by 2