Sgardioli IC, Molck MC, Copelli M de M, Vieira TAP, Gil da Silva Lopes VL. Loss of heterozygosity (LOH) Analysis in individuals with developmental delay/congenital anomalies previously investigated for 22q11.2 Deletion Syndrome. Semin. Cienc. Biol. Saude [Internet]. 16º de fevereiro de 2018 [citado 21º de novembro de 2024];38(1supl):198. Disponível em: https://ojs.uel.br/revistas/uel/index.php/seminabio/article/view/29486