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	1.	Unique Combination of 22q11 and 14qter Microdeletion Syndromes Detected Using Oligonucleotide Array-CGH. [electronic resource] by Zrnová, E Vranová, V Soukalová, J Slámová, I Vilémová, M Gaillyová, R Kuglík, P Publication details: Molecular syndromology Jan 2012 In: Molecular syndromology vol. 2 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	SHOX gene defects and selected dysmorphic signs in patients of idiopathic short stature and Léri-Weill dyschondrosteosis. [electronic resource] by Hirschfeldova, K Solc, R Baxova, A Zapletalova, J Kebrdlova, V Gaillyova, R Prasilova, S Soukalova, J Mihalova, R Lnenicka, P Florianova, M Stekrova, J Producer: 20120118 In: Gene vol. 491 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	[Identification of a Family with SUFU Germline Deletion Based on a Case of Desmoplastic Medulloblastoma in an Infant]. [electronic resource] by Šoukalová, J Vejmělková, K Cermanová, T Kašíková, K Mikulášová, A Janyšková, H Melichárková, K Pavelka, Z Ježová, M Pospíšilová, Š Kuglík, P Valášková, I Gaillyová, R Štěrba, J Zitterbart, K Producer: 20160307 In: Klinicka onkologie : casopis Ceske a Slovenske onkologicke spolecnosti vol. 29 Suppl 1 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)