Výsledky vyhľadávania
- 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
- C 526
- 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]