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Paper Details

De Novo and Inherited Loss-of-Function Variants in TLK2: Clinical and Genotype-Phenotype Evaluation of a Distinct Neurodevelopmental Disorder.
Am J Hum Genet
28
2018
Author NameAffiliation
Anna de BurcaOxford University Hospitals NHS Foundation Trust
Bert B A de VriesDonders Institute for Brain, Radboud University Medical Center
Charu DeshpandeGuy's Hospital
Jill Clayton-SmithUniversity of Manchester, Manchester University Hospitals NHS Foundation Trust
Kelly RadtkeDivision of Clinical Genomics
Tim M StromInstitute of Human Genetics, Germany Institute of Human Genetics, Technische Universitat Munchen
Maria Bitner-GlindziczUCL Great Ormond Street Institute of Child Health
Lauren BrickMcMaster Children's Hospital, McMaster University
Mariya KozenkoMcMaster Children's Hospital, McMaster University
Sofia DouzgouUniversity of Manchester, Manchester University Hospitals NHS Foundation Trust
Nils KoellingClinical Genetics Group, MRC Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital
Christoffer Nell??kerUniversity of Oxford, John Radcliffe Hospital, UK Institute of Biomedical Engineering, UK Big Data Institute
Han G BrunnerDonders Institute for Brain, Radboud University Medical Center, Maastricht University Medical Center
Andrew O M WilkieClinical Genetics Group, MRC Weatherall Institute of Molecular Medicine, University of Oxford, John Radcliffe Hospital, Oxford University Hospitals NHS Trust
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