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  1. 1.De novo mutations of GCK, HNF1A and HNF4A may be more frequent in MODY than previously assumed

    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]
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  2. 2.Lessons from 30 years of clinical diagnosis and treatment of congenital adrenal hyperplasia in five middle European countries

    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]
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