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	1.	[Detection and diagnosis of hereditary monogenic neurologic diseases in Slovakia]. [electronic resource] by Jurasova, A Traubner, P Behulova, R Mezenska, R Lukacova, M Producer: 20000615 In: Bratislavske lekarske listy vol. 101 Availability: No items available. Save to lists Add to cart (remove)
	2.	[Presence of Y-specific sequences in patients with Turner syndrome as a presymptomatic marker of increased risk of gonadoblastoma]. [electronic resource] by Horváthová, L Mezenská, R Mináriková, O Véghová, E Lukácová, M Simko, J Producer: 19980617 In: Bratislavske lekarske listy vol. 99 Availability: No items available. Save to lists Add to cart (remove)
	3.	[Indirect diagnosis of type I neurofibromatosis using RFLP in Slovak families]. [electronic resource] by Mezenska, R Durovcikova, D Behulova, R Lukacova, M Lozsekova, A Simko, J Producer: 20000720 In: Bratislavske lekarske listy vol. 101 Availability: No items available. Save to lists Add to cart (remove)
	4.	[Diagnosis of Duchenne and Becker muscular dystrophy in Slovak patients using multiplex polymerase chain reaction]. [electronic resource] by Simko, J Zatkalíková, L Mezenská, R Behulová, R Mináriková, O Simko, F Producer: 19980826 In: Bratislavske lekarske listy vol. 99 Availability: No items available. Save to lists Add to cart (remove)
	5.	[Y-chromosome mosaicism as markers of increased risk for development of gonadoblastoma in patients with Turner's syndrome]. [electronic resource] by Simko, J Horváthová, L Mezenská, R Lukácová, M Holomán, K I Simko, F Producer: 19970916 In: Ceska gynekologie vol. 62 Availability: No items available. Save to lists Add to cart (remove)
	6.	PCR based diagnosis of 21-hydroxylase gene defects in Slovak patients with congenital adrenal hyperplasia. [electronic resource] by Pinterova, L Garami, M Pribilincova, Z Behulova, R Mezenska, R Lukacova, M Zorad, S Producer: 20000914 In: Endocrine regulations vol. 34 Availability: No items available. Save to lists Add to cart (remove)
	7.	[Use of variable number of tandem repeat polymorphism in assessing correct sampling in prenatal diagnosis of monogenic disorders]. [electronic resource] by Simko, J Zatkalíková, L Mezenská, R Mináriková, O Behulová, R Holomán, K I Krizko, M Simko, F Producer: 19980820 In: Ceska gynekologie vol. 63 Availability: No items available. Save to lists Add to cart (remove)