Search Results - Sadikovic, Bekim
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DNA methylation episignature, extension of the clinical features, and comparative epigenomic profiling of Hao-Fountain syndrome caused by variants in USP7 by Laan, Liselot van der (Author) , Karimi, Karim (Author) , Rooney, Kathleen (Author) , Lauffer, Peter (Author) , McConkey, Haley (Author) , Caro, Pilar (Author) , Relator, Raissa (Author) , Levy, Michael A. (Author) , Bhai, Pratibha (Author) , Mignot, Cyril (Author) , Keren, Boris (Author) , Briuglia, Silvana (Author) , Sobering, Andrew K. (Author) , Li, Dong (Author) , Vissers, Lisenka E. L. M. (Author) , Dingemans, Alexander J. M. (Author) , Valenzuela, Irene (Author) , Verberne, Eline A. (Author) , Misra-Isrie, Mala (Author) , Zwijnenburg, Petra J. G. (Author) , Waisfisz, Quinten (Author) , Alders, Mariëlle (Author) , Sailer, Sebastian (Author) , Schaaf, Christian P. (Author) , Mannens, Marcel M. A. M. (Author) , Sadikovic, Bekim (Author) , van Haelst, Mieke M. (Author) , Henneman, Peter (Author) ,
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Abnormalities, Multiple
Autism Spectrum Disorder
Biomarkers
Bone Diseases, Developmental
Craniofacial Abnormalities
DNA Methylation
DNA methylation
Deafness
Epigenomics
Episignature
Hao-Fountain syndrome
Humans
Intellectual Disability
Intellectual disability
Neurodevelopmental Disorders
Phenotype
USP7
Ubiquitin-Specific Peptidase 7