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, Elizabeth Roeder, Rebecca O. Littlejohn et al.|Genome Medicine|2019Cited by 48
Two de novo novel mutations in one <i>SHANK3</i> allele in a patient with autism and moderate intellectual disabilityWenmiao Zhu, Weimin Bi, Jianli Li et al.|American Journal of Medical Genetics Part A|2018Cited by 10
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