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GPR143 gene mutation analysis in pediatric patients with albinism.
Trebušak Podkrajšek K, Stirn Kranjc B, Hovnik T, Kovač J, Battelino T. Trebušak Podkrajšek K, et al. Among authors: stirn kranjc b. Ophthalmic Genet. 2012 Sep;33(3):167-70. doi: 10.3109/13816810.2011.559651. Epub 2012 Apr 9. Ophthalmic Genet. 2012. PMID: 22486324
Refining clinical phenotypes in septo-optic dysplasia based on MRI findings.
Riedl S, Vosahlo J, Battelino T, Stirn-Kranjc B, Brugger PC, Prayer D, Müllner-Eidenböck A, Kapelari K, Blümel P, Waldhör T, Krasny J, Lebl J, Frisch H. Riedl S, et al. Among authors: stirn kranjc b. Eur J Pediatr. 2008 Nov;167(11):1269-76. doi: 10.1007/s00431-007-0666-x. Epub 2008 Jan 30. Eur J Pediatr. 2008. PMID: 18231810
Chromatic VEP in children with congenital colour vision deficiency.
Tekavčič Pompe M, Stirn Kranjc B, Brecelj J. Tekavčič Pompe M, et al. Among authors: stirn kranjc b. Ophthalmic Physiol Opt. 2010 Sep;30(5):693-8. doi: 10.1111/j.1475-1313.2010.00739.x. Ophthalmic Physiol Opt. 2010. PMID: 20883356
25 results