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	1.	Elejalde syndrome--a case report. [electronic resource] by Silhánová, Eva Plevová, Pavlína Curík, Romuald Kaspercík, Ivo Krepelová, Anna Producer: 20061213 In: American journal of medical genetics. Part A vol. 140 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Molecular and clinical characterization of two patients with Prader-Willi syndrome and atypical deletions of proximal chromosome 15q. [electronic resource] by Calounova, Gabriela Hedvicakova, Petra Silhanova, Eva Kreckova, Gabriela Sedlacek, Zdenek Producer: 20080819 In: American journal of medical genetics. Part A vol. 146A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	High incidence of monozygotic twinning after assisted reproduction is related to genetic information, but not to assisted reproduction technology itself. [electronic resource] by Sobek, Aleš Zbořilová, Blažena Procházka, Martin Šilhánová, Eva Koutná, Olga Klásková, Eva Tkadlec, Emil Sobek, Aleš Producer: 20160303 In: Fertility and sterility vol. 103 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Associations between congenital heart defects and genetic and morphological anomalies. The importance of prenatal screening. [electronic resource] by Pavlicek, Jan Gruszka, Tomas Kapralova, Sabina Prochazka, Martin Silhanova, Eva Kaniova, Romana Polanska, Slavka Cernickova, Renata Klaskova, Eva Producer: 20190902 In: Biomedical papers of the Medical Faculty of the University Palacky, Olomouc, Czechoslovakia vol. 163 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)