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	1.	Distribution of 9 common mutations in the CFTR gene in Slovak cystic fibrosis patients. [electronic resource] by Kádasi, L Poláková, H Zatková, A Kayserová, H Producer: 19980803 In: Gene geography : a computerized bulletin on human gene frequencies vol. 11 Availability: No items available. Save to lists Add to cart (remove)
	2.	Rapid detection methods for five HGO gene mutations causing alkaptonuria. [electronic resource] by Zatkova, A Chmelikova, A Polakova, H Ferakova, E Kadasi, L Producer: 20031027 In: Clinical genetics vol. 63 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	[The spectrum of mutations in the CFTR gene in patients with cystic fibrosis in Slovakia]. [electronic resource] by Kádasi, L Poláková, H Zatková, A Kayserová, H Hruskovic, I Producer: 19980617 In: Bratislavske lekarske listy vol. 99 Availability: No items available. Save to lists Add to cart (remove)
	4.	Early-onset ocular ochronosis in a girl with alkaptonuria (AKU) and a novel mutation in homogentisate 1,2-dioxygenase (HGD). [electronic resource] by Gucev, Z S Slaveska, N Laban, N Danilovski, D Tasic, V Pop-Jordanova, N Zatkova, A Producer: 20160401 In: Prilozi vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	5.	Novel mutations in the homogentisate-1,2-dioxygenase gene identified in Slovak patients with alkaptonuria. [electronic resource] by Zatková, A Polaková, H Micutková, L Zvarík, M Bosák, V Feráková, E Matusek, J Ferák, V Kádasi, L Producer: 20000828 In: Journal of medical genetics vol. 37 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	Two sporadic spinal neurofibromatosis patients with malignant peripheral nerve sheath tumour. [electronic resource] by Fauth, C Kehrer-Sawatzki, H Zatkova, A Machherndl-Spandl, S Messiaen, L Amann, G Hainfellner, J A Wimmer, K Producer: 20100201 In: European journal of medical genetics vol. 52 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	High frequency of alkaptonuria in Slovakia: evidence for the appearance of multiple mutations in HGO involving different mutational hot spots. [electronic resource] by Zatková, A de Bernabé, D B Poláková, H Zvarík, M Feráková, E Bosák, V Ferák, V Kádasi, L de Córdoba, S R Producer: 20001214 In: American journal of human genetics vol. 67 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	Clustering of mutations in the 5' tertile of the NF1 gene in Slovakia patients with optic pathway glioma. [electronic resource] by Bolcekova, A Nemethova, M Zatkova, A Hlinkova, K Pozgayova, S Hlavata, A Kadasi, L Durovcikova, D Gerinec, A Husakova, K Pavlovicova, Z Holobrada, M Kovacs, L Ilencikova, D Producer: 20131114 In: Neoplasma vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	RNA-based mutation analysis identifies an unusual MSH6 splicing defect and circumvents PMS2 pseudogene interference. [electronic resource] by Etzler, J Peyrl, A Zatkova, A Schildhaus, H-U Ficek, A Merkelbach-Bruse, S Kratz, C P Attarbaschi, A Hainfellner, J A Yao, S Messiaen, L Slavc, I Wimmer, K Producer: 20080207 In: Human mutation vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)