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	1.	[A clinical and molecular genetic analysis of the fragile X syndrome]. [electronic resource] by Bychkova, A M Maliarchuk, S G Livshits, L A Producer: 19991130 In: TSitologiia i genetika vol. 33 Availability: No items available. Save to lists Add to cart (remove)
	2.	[The role of ultrasonic and cytogenetic markers in prenatal diagnostics]. [electronic resource] by Sopko, N I Tavokina, L V Buĭnova, V A Bychkova, A M Producer: 20070212 In: TSitologiia i genetika vol. 40 Availability: No items available. Save to lists Add to cart (remove)
	3.	[The clinical and molecular genetic characteristics of phenylketonuria patients in the Republic of Crimea]. [electronic resource] by Afanas'eva, N A Bychkova, A M Livshits, L A Bariliak, I R Producer: 19980904 In: TSitologiia i genetika vol. 32 Availability: No items available. Save to lists Add to cart (remove)
	4.	Prognosis of probability of BRCA1 and BRCA2 mutations carriage in women with compromised family history of breast and/or ovarian cancer. [electronic resource] by Rybchenko, L A Bychkova, A M Skyban, G V Klymenko, S V Producer: 20150205 In: Problemy radiatsiinoi medytsyny ta radiobiolohii no. 18 Availability: No items available. Save to lists Add to cart (remove)
	5.	[A case pf spontaneous deletion in the FMR1 gene in a patient with the Martin-Bell syndrome]. [electronic resource] by Maliarchuk, S G Bychkova, A M Lee, S Verteletskiĭ, V Livshits, L A Producer: 19971124 In: TSitologiia i genetika vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	6.	[Methylation status of the FMR1 gene promotor in patients with Martin-Bell syndrome from Ukraine]. [electronic resource] by Grishchenko, N V Maliarchuk, S G Ekshiian, A Iu Bychkova, A M Livshits, L A Producer: 20021120 In: TSitologiia i genetika vol. 36 Availability: No items available. Save to lists Add to cart (remove)
	7.	[A molecular genetic analysis of spinal muscular atrophy (SMA) in families at high risk from different regions of Ukraine]. [electronic resource] by Ekshiian, A Iu Livshits, L A Bychkova, A M Afanas'eva, N A Bariliak, I R Producer: 19980701 In: TSitologiia i genetika vol. 31 Availability: No items available. Save to lists Add to cart (remove)
	8.	[Study of the duplication of 17p11.2-12 chromosome region in the patients with hereditary motor and sensory neuropathy type 1A]. [electronic resource] by Hryshchenko, N V Bychkova, A M Pichkur, N A Skyban, H V Dmytrenko, V V Livshyts', L A Producer: 20040621 In: TSitologiia i genetika vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	9.	[A case of deletion of the short arm of the chromosome 21 (21p-) (christchurch chromosome) discovered prenatally:clinical and cytogenetic data]. [electronic resource] by Tavokina, L V Vorsanova, S G Zukin, V D Sopko, N I Zinchenko, V M Veselovskiĭ, V V Bychkova, A M Nikitchina, T V Iurov, Iu B Producer: 20040827 In: TSitologiia i genetika vol. 38 Availability: No items available. Save to lists Add to cart (remove)
	10.	[Molecular diagnosis of fragile X-chromosome syndrome (Martin-Bell syndrome) in patients of native populations]. [electronic resource] by Baranov, V S Aseev, M V Rakisheva, Z B Kuleshov, N P Marinicheva, G S Bychkova, A M Zukin, V D Ledashcheva, E A Amoashiĭ, D S Kuznetsova, T V Producer: 19931012 In: Genetika vol. 29 Availability: No items available. Save to lists Add to cart (remove)