Výsledky vyhľadávania
- 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]