[1]
Sgardioli, I.C. et al. 2018. Loss of heterozygosity (LOH) Analysis in individuals with developmental delay/congenital anomalies previously investigated for 22q11.2 Deletion Syndrome. Semina: Ciências Biológicas e da Saúde. 38, 1supl (fev. 2018), 198. DOI:https://doi.org/10.5433/1679-0367.2017v38n1suplp198.