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	1.	Molecular Screening of Keratoconus Susceptibility Sequence Variants in VSX1, TGFBI, DOCK9, STK24, and IPO5 Genes in Polish Patients and Novel TGFBI Variant Identification. [electronic resource] by Karolak, Justyna A Polakowski, Piotr Szaflik, Jerzy Szaflik, Jacek P Gajecka, Marzena Producer: 20160914 In: Ophthalmic genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	IGF-1 gene polymorphisms in Polish families with high-grade myopia. [electronic resource] by Rydzanicz, Malgorzata Nowak, Dorota M Karolak, Justyna A Frajdenberg, Agata Podfigurna-Musielak, Monika Mrugacz, Malgorzata Gajecka, Marzena Producer: 20120126 In: Molecular vision vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	3.	Substitution at IL1RN and deletion at SLC4A11 segregating with phenotype in familial keratoconus. [electronic resource] by Nowak, Dorota M Karolak, Justyna A Kubiak, Joanna Gut, Marta Pitarque, Jose A Molinari, Andrea Bejjani, Bassem A Gajecka, Marzena Producer: 20130514 In: Investigative ophthalmology & visual science vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Sequence variants in COL4A1 and COL4A2 genes in Ecuadorian families with keratoconus. [electronic resource] by Karolak, Justyna A Kulinska, Karolina Nowak, Dorota M Pitarque, Jose A Molinari, Andrea Rydzanicz, Malgorzata Bejjani, Bassem A Gajecka, Marzena Producer: 20110908 In: Molecular vision vol. 17 Availability: No items available. Save to lists Add to cart (remove)
	5.	Novel mutation and three other sequence variants segregating with phenotype at keratoconus 13q32 susceptibility locus. [electronic resource] by Czugala, Marta Karolak, Justyna A Nowak, Dorota M Polakowski, Piotr Pitarque, Jose Molinari, Andrea Rydzanicz, Malgorzata Bejjani, Bassem A Yue, Beatrice Y J T Szaflik, Jacek P Gajecka, Marzena Producer: 20120803 In: European journal of human genetics : EJHG vol. 20 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Deletions and duplications of developmental pathway genes in 5q31 contribute to abnormal phenotypes. [electronic resource] by Rosenfeld, Jill A Drautz, Joanne Milisa Clericuzio, Carol L Cushing, Tom Raskin, Salmo Martin, Judith Tervo, Raymond C Pitarque, Jose A Nowak, Dorota M Karolak, Justyna A Lamb, Allen N Schultz, Roger A Ballif, Blake C Bejjani, Bassem A Gajecka, Marzena Shaffer, Lisa G Producer: 20111123 In: American journal of medical genetics. Part A vol. 155A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)