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  1. Genotyping patients with fatty acid oxidation defects: Why, when and how  / N. Gregersen, B.S. Andresen .  Bratislavské lekárske listy : international journal for biomedical sciences and clinical medicine. - ISSN 0006-9248 . - Vol. 105, no. 9 (2004), s. 323  
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  2. Six novel mutations in the arginine vasopressin gene in 15 kindreds with autosomal dominant familial neurohypophyseal diabetes insipidus give further insight into the pathogenesis  / Kovacs, L. ... [et al.] .  European journal of human genetics . - Vol. 12, no. 1 (2004), pp. 44–51   [Dokument nie je vo fonde knižnice]
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