Associated Papers
Two families with TET3-related disorder showing neurodevelopmental delay with craniofacial dysmorphisms.
Seyama R et al.
Journal of Human Genetics, 2022
Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders.
Levy MA et al.
Hgg Advances, 2022
35047860 (PubMed )
Supplement: mmc2.xlsx › Table_S1_samples
Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood.
Levy MA et al.
Npj Genomic Medicine, 2021
Novel candidate genes and variants underlying autosomal recessive neurodevelopmental disorders with intellectual disability.
Santos-Cortez RLP et al.
Human Genetics, 2018
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