Associated Papers
Analysis of exome data in a UK cohort of 603 patients with syndromic orofacial clefting identifies causal molecular pathways.
Wilson K et al.
Human Molecular Genetics, 2023
37010288 (PubMed )
Supplement: supptables_hmg-2022-ce-00520-r1_wilson_without_id_ddad023.xlsx › S4
Report of two children with global developmental delay in association with de novo TLK2 variant and literature review.
Woods E et al.
American Journal of Medical Genetics. Part A, 2022
The Tousled-like kinases regulate genome and epigenome stability: implications in development and disease.
Segura-Bayona S et al.
Cellular and Molecular Life Sciences : Cmls, 2019
De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder.
Reijnders MRF et al.
American Journal of Human Genetics, 2018
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