[1]
Moufid, F.Z. et al. 2018. Molecular and presymptomatic analysis of a Moroccan Lynch syndrome family revealed a novel frameshift MLH1 germline mutation. Turkish Journal of Gastroenterology. 29, 6 (Jan. 2018), 701–704. DOI:https://doi.org/10.5152/tjg.2018.17761.