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Casini, A; Sokollik, Christiane; Lukowski, S W; Lurz, E; Rieubland, C; de Moerloose, P; Neerman-Arbez, M (2015). Hypofibrinogenemia and liver disease: a new case of Aguadilla fibrinogen and review of the literature. Haemophilia, 21(6), pp. 820-827. Blackwell Science 10.1111/hae.12719
Bruno, D L; Ganesamoorthy, D; Schoumans, J; Bankier, A; Coman, D; Delatycki, M; Gardner, R J M; Hunter, M; James, P A; Kannu, P; McGillivray, G; Pachter, N; Peters, H; Rieubland, C; Savarirayan, R; Scheffer, I E; Sheffield, L; Tan, T; White, S M; Yeung, A; ... (2009). Detection of cryptic pathogenic copy number variations and constitutional loss of heterozygosity using high resolution SNP microarray analysis in 117 patients referred for cytogenetic analysis and impact on clinical practice. Journal of medical genetics, 46(2), pp. 123-31. London: BMJ Publishing Group 10.1136/jmg.2008.062604
Radan, Anda-Petronela; Mosimann, Beatrice; Trottmann, Fabienne; Rieubland, C; Surbek, Daniel; Raio, Luigi (2020). Arthrogryposis multiplex congenita: fetal sonographic, clinical and genetic findings in seven cases from a tertiary care center in Switzerland (Unpublished). In: Care center in Switzerland.
