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, Andrea M. Lewis, Kimberly Nugent 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