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Niedrist, D; Joncourt, F; Mátyás, G; Müller, A (2009). Severe phenotype with cis-acting heterozygous PMP22 mutations. Clinical genetics, 75(3), pp. 286-9. Oxford: Wiley-Blackwell 10.1111/j.1399-0004.2008.01120.x
Ramelli, G P; Joncourt, F; Luetschg, J; Weis, J; Tolnay, M; Burgunder, J M (2006). Becker muscular dystrophy with marked divergence between clinical and molecular genetic findings: case series. Swiss medical weekly, 136(11-12), pp. 189-93. Muttenz: EMH Schweizerischer Ärzteverlag
