Phenotypic expansion in <i> <scp>DDX</scp> 3X </i> – a common cause of intellectual disability in femalesXia Wang, Paolo Moretti, Theresa Mihalic Mosher et al.|Annals of Clinical and Translational Neurology|2018Cited by 91
De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndromeSarah H. Elsea, Francesco Vetrini, Shane McKee et al.|Genome Medicine|2019Cited by 48
Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith–Magenis syndromeSarah H. Elsea, Francesco Vetrini, Shane McKee et al.|Genome Medicine|2019Cited by 2
Correction to: De novo and inherited TCF20 pathogenic variants are associated with intellectual disability, dysmorphic features, hypotonia, and neurological impairments with similarities to Smith-Magenis syndromeFrancesco Vetrini, Jennifer E. Posey, Shane McKee et al.|PMC|2019Cited by 1
Phenotypic expansion in <i>DDX3X</i> – a common cause of intellectual disability in femalesXia Wang, Paolo Moretti, Jill A. Rosenfeld et al.|bioRxiv (Cold Spring Harbor Laboratory)|2018Cited by 0