Associated Papers
Different Contribution of Missense and Loss-of-Function Variants to the Genetic Structure of Familial and Sporadic Meniere Disease.
Parra-Perez AM et al.
Medcomm, 2025
40989574 (PubMed )
Supplement: MCO2-6-e70394-s001.xlsx › TableS15
Whole exome sequencing in 18 Brazilian families with vertical transmission of non-syndromic oral clefts.
Copelli MM et al.
Journal of Cranio-maxillo-facial Surgery : Official Publication of the European Association for Cranio-maxillo-facial Surgery, 2025
Four putative pathogenic ARHGAP29 variants in patients with non-syndromic orofacial clefts (NsOFC).
Ranji P et al.
European Journal of Human Genetics : Ejhg, 2025
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