[1]
Argyriou, L., Wirbelauer, J., Dev, A., Panchulidze, I., Shoukier, M., Teske, U. and Nayernia, K. 2008. A newborn with hereditary haemorrhagic telangiectasia and an unusually severe phenotype. Swiss Medical Weekly. 138, 2930 (Jul. 2008), 432–435. DOI:https://doi.org/10.4414/smw.2008.12135.