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Molecular Vision|November 6, 2007
TGFBI (BIGH3) gene mutations in Hungary--report of the novel F547S mutation associated with polymorphic corneal amyloidosisLili Takács, Gergely Losonczy, Klára Matesz, et al.
Blood|January 11, 2014
Interaction of factor XIII subunitsEva Katona, Krisztina Pénzes, Andrea Csapó, et al.
European Journal of Endocrinology|July 4, 2009
Germline VHL gene mutations in Hungarian families with von Hippel-Lindau disease and patients with apparently sporadic unilateral pheochromocytomasPeter Gergics, Attila Patocs, Miklos Toth, et al.
Cytometry. Part a : the Journal of the International Society for Analytical Cytology|January 22, 2008
Heteroduplex analysis using flow cytometric microbead assays to detect deletions, insertions, and single-strand lesionsEva Hegedüs, László Imre, Judit Pataki, et al.
Human Mutation|May 18, 2004
GJB2 mutations in patients with non-syndromic hearing loss from Northeastern HungaryTímea Tóth, Susan Kupka, Birgit Haack, et al.
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