Associated Papers
An intragenic duplication in the AFF2 gene associated with Cornelia de Lange syndrome phenotype.
Lucia-Campos C et al.
Frontiers in Genetics, 2024
39553472 (PubMed )
Supplement: Table2.XLSX › Supplementary_Table_1
AFF2 Is Associated With X-Linked Partial (Focal) Epilepsy With Antecedent Febrile Seizures.
Zou D et al.
Frontiers in Molecular Neuroscience, 2022
An international telemedicine program for diagnosis of genetic disorders: Partnership of pediatrician and geneticist.
Mena R et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics, 2020
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