Authors: Neerman-Arbez, M de Moerloose, P Honsberger, A Parlier, G Arnuti, B Biron, C Borg, JY Eber, S Meili, E Peter-Salonen, K Ripoll, L Vervel, C d'Oiron, R Staeger, P Antonarakis, SE Morris, MA

Citation: M. Neerman-arbez et al., Molecular analysis of the fibrinogen gene cluster in 16 patients with congenital afibrinogenemia: novel truncating mutations in the FGA and FGG genes, HUM GENET, 108(3), 2001, pp. 237-240

Authors: Wilmer, M Rudin, K Kolde, HJ Poetzsch, B Lenz, W Moessmer, G Meili, E Egbring, R Gempeler-Messina, P Gempeler, M Bastian, S Kohler, HP

Citation: M. Wilmer et al., Evaluation of a sensitive colorimetric FXIII incorporation assay. Effects of FXIII Val34Leu, plasma fibrinogen concentration and congenital FXIII deficiency, THROMB RES, 102(1), 2001, pp. 81-91

Authors: Millar, DS Kemball-Cook, G McVey, JH Tuddenham, EGD Mumford, AD Attock, GB Reverter, JC Lanir, N Parapia, LA Reynaud, J Meili, E von Felton, A Martinowitz, U Prangnell, DR Krawczak, M Cooper, DN

Citation: Ds. Millar et al., Molecular analysis of the genotype-phenotype relationship in factor VII deficiency, HUM GENET, 107(4), 2000, pp. 327-342

Authors: Schmid, C Meili, E

Citation: C. Schmid et E. Meili, Acromegaly in a hemophilic patient infected with the hepatitis C and humanimmunodeficiency viruses, AM J MED, 108(9), 2000, pp. 757-758