Associated Papers
Phenotypic spectrum of the RBM10-mediated intellectual disability and congenital malformation syndrome beyond classic TARP syndrome features.
Kumps C et al.
Clinical Genetics, 2021
A novel missense variant in RBM10 can cause a mild form of TARP syndrome with developmental delay and dysmorphic features.
Imagawa E et al.
Clinical Genetics, 2020
Infant male with TARP syndrome: Review of clinical features, prognosis, and commonalities with previously reported patients.
Kaeppler KE et al.
American Journal of Medical Genetics. Part A, 2018
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