Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic featuresJing Zhang, Paweł Stankiewicz, Aisha M. Al Shamsi et al.|Human Genetics|2017Cited by 65
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
Erratum to: Haploinsufficiency of the E3 ubiquitin-protein ligase gene TRIP12 causes intellectual disability with or without autism spectrum disorders, speech delay, and dysmorphic featuresJing Zhang, Paweł Stankiewicz, Tomasz Gambin et al.|Human Genetics|2017Cited by 5
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