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	1.	[Genetic basis of hereditary optic atrophies]. [electronic resource] by Wawrocka, Anna Krawczyński, Maciej R Producer: 20080617 In: Klinika oczna vol. 109 Availability: No items available. Save to lists Add to cart (remove)
	2.	11p13 deletions can be more frequent than the PAX6 gene point mutations in Polish patients with aniridia. [electronic resource] by Wawrocka, Anna Sikora, Agata Kuszel, Lukasz Krawczynski, Maciej R Producer: 20140114 In: Journal of applied genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Severe manifestation of Leber's hereditary optic neuropathy due to 11778G>A mtDNA mutation in a female with hypoestrogenism due to Perrault syndrome. [electronic resource] by Badura-Stronka, Magdalena Wawrocka, Anna Zawieja, Krzysztof Silska, Sylwia Krawczyński, Maciej Robert Producer: 20140715 In: Mitochondrion vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	PAX6 3' deletion in a family with aniridia. [electronic resource] by Wawrocka, Anna Budny, Bartlomiej Debicki, Szymon Jamsheer, Aleksander Sowinska, Anna Krawczynski, Maciej Robert Producer: 20120329 In: Ophthalmic genetics vol. 33 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Granular corneal dystrophy in 830-nm spectral optical coherence tomography. [electronic resource] by Kaluzny, Bartlomiej J Szkulmowska, Anna Szkulmowski, Maciej Bajraszewski, Tomasz Wawrocka, Anna Krawczynski, Maciej R Kowalczyk, Andrzej Wojtkowski, Maciej Producer: 20080821 In: Cornea vol. 27 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)