Associated Papers
Rare Variant Burden and Behavioral Phenotypes in Children with Autism in Slovakia.
Repiská G et al.
Genes, 2025
40869941 (PubMed )
Supplement: genes-16-00893-s001.zip › File_S1.xlsx › suplement
Monogenic Forms of DSD: An Update.
McElreavey K et al.
Hormone Research in Paediatrics, 2023
Neurological Disorders Associated with WWOX Germline Mutations-A Comprehensive Overview.
Banne E et al.
Cells, 2021
33916893 (PubMed )
Supplement: cells-10-00824-s001.zip › supplementary_materials › Table_2_SuppInfo_Clinvar_Uncertain_significance_variants_that_linked_to_WOREE_and_SCAR12_.xlsx › Uncertain_significance_variants
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