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	1.	[Formation of congenital defects during ocular development. I. Embryogenesis of the eye and developmental birth defects]. [electronic resource] by Krawczyński, Maciej R Producer: 20040517 In: Klinika oczna vol. 105 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Genetic ground of primary open angle glaucoma]. [electronic resource] by Krawczyński, Maciej R Producer: 20050510 In: Klinika oczna vol. 106 Availability: No items available. Save to lists Add to cart (remove)
	3.	[Formation of congenital defects during ocular development. II. Genetic background of oculogenesis and developmental birth defects]. [electronic resource] by Krawczyński, Maciej R Producer: 20040517 In: Klinika oczna vol. 105 Availability: No items available. Save to lists Add to cart (remove)
	4.	Four novel RS1 gene mutations in Polish patients with X-linked juvenile retinoschisis. [electronic resource] by Skorczyk, Anna Krawczyński, Maciej R Producer: 20130514 In: Molecular vision vol. 18 Availability: No items available. Save to lists Add to cart (remove)
	5.	PCD and RP: X-linked inheritance of both disorders? [electronic resource] by Krawczyński, Maciej R Witt, Michał Producer: 20041026 In: Pediatric pulmonology vol. 38 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	[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)
	7.	Apparent X-linked primary ciliary dyskinesia associated with retinitis pigmentosa and a hearing loss. [electronic resource] by Krawczyński, Maciej R Dmeńska, Hanna Witt, Michał Producer: 20040414 In: Journal of applied genetics vol. 45 Availability: No items available. Save to lists Add to cart (remove)
	8.	m.3635G>A mutation as a cause of Leber hereditary optic neuropathy. [electronic resource] by Kodroń, Agata Krawczyński, Maciej R Tońska, Katarzyna Bartnik, Ewa Producer: 20140815 In: Journal of clinical pathology vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	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)
	10.	[Study of TIGR gene in patients with primary open angle glaucoma]. [electronic resource] by Krawczyński, Maciej R Czarny-Ratajczak, Malwina Pecold, Krystyna Latos-Bieleńska, Anna Producer: 20050510 In: Klinika oczna vol. 106 Availability: No items available. Save to lists Add to cart (remove)
	11.	Only neutral polymorphisms found in the TIGR/myocilin gene of 45 Polish patients with primary open-angle glaucoma. [electronic resource] by Krawczyński, Maciej R Czarny-Ratajczak, Malwina Pecold, Krystyna Latos-Bieleńska, Anna Producer: 20040629 In: Journal of applied genetics vol. 45 Availability: No items available. Save to lists Add to cart (remove)
	12.	A novel mitochondrial DNA deletion in a patient with Kearns-Sayre syndrome: a late-onset of the fatal cardiac conduction deficit and cardiomyopathy accompanying long-term rGH treatment. [electronic resource] by Obara-Moszynska, Monika Maceluch, Jaroslaw Bobkowski, Waldemar Baszko, Artur Jaremba, Oskar Krawczynski, Maciej R Niedziela, Marek Producer: 20130621 In: BMC pediatrics vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	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)
	14.	Frequency of 22q11.2 microdeletion in children with congenital heart defects in western poland. [electronic resource] by Wozniak, Anna Wolnik-Brzozowska, Danuta Wisniewska, Marzena Glazar, Renata Materna-Kiryluk, Anna Moszura, Tomasz Badura-Stronka, Magdalena Skolozdrzy, Joanna Krawczynski, Maciej R Zeyland, Joanna Bobkowski, Waldemar Slomski, Ryszard Latos-Bielenska, Anna Siwinska, Aldona Producer: 20110810 In: BMC pediatrics vol. 10 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)