Výsledky vyhľadávania
- De novo mutations of GCK, HNF1A and HNF4A may be more frequent in MODY than previously assumed / Staník J. [et al.] . Diabetologia. - ISSN 0012-186X . - Vol. 57, no. 3 (2014), p. 480-484 [Dokument nie je vo fonde knižnice]
- Lessons from 30 years of clinical diagnosis and treatment of congenital adrenal hyperplasia in five middle European countries / Kovács J. ... [et al.] . The Journal of clinical endocrinology and metabolism . - Vol. 86, no. 7 (2001), s. 2958-2964 [Dokument nie je vo fonde knižnice]