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	1.	Prenatal diagnosis of Pallister-Killian syndrome in pregnancy with normal CVS result and abnormal ultrasound findings in the second trimester. [electronic resource] by Frisova, Veronika Svobodova, Ivana Tutkova Tozzi, Michaela Raskova, Dagmar Producer: 20190117 In: Taiwanese journal of obstetrics & gynecology vol. 57 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	Early detection of bilateral cataracts in utero may represent a manifestation of severe congenital disease. [electronic resource] by Trkova, Marie Hynek, Martin Dudakova, Lubica Becvarova, Vera Hlozanek, Martin Raskova, Dagmar Vincent, Andrea L Liskova, Petra Producer: 20171023 In: American journal of medical genetics. Part A vol. 170 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	STRC Gene Mutations, Mainly Large Deletions, are a Very Important Cause of Early-Onset Hereditary Hearing Loss in the Czech Population. [electronic resource] by Marková, Simona Poisson Brožková, Dana Šafka Laššuthová, Petra Mészárosová, Anna Krůtová, Marcela Neupauerová, Jana Rašková, Dagmar Trková, Marie Staněk, David Seeman, Pavel Producer: 20180727 In: Genetic testing and molecular biomarkers vol. 22 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	Spectrum and frequency of SLC26A4 mutations among Czech patients with early hearing loss with and without Enlarged Vestibular Aqueduct (EVA). [electronic resource] by Pourová, Radka Janousek, Petr Jurovcík, Michal Dvoráková, Marcela Malíková, Marcela Rasková, Dagmar Bendová, Olga Leonardi, Emanuela Murgia, Alessandra Kabelka, Zdenek Astl, Jaromír Seeman, Pavel Producer: 20100805 In: Annals of human genetics vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene. [electronic resource] by Čada, Zdeněk Šafka Brožková, Dana Balatková, Zuzana Plevová, Pavlína Rašková, Dagmar Laštůvková, Jana Černý, Rudolf Bandúrová, Veronika Koucký, Vladimír Hrubá, Silvie Komarc, Martin Jenčík, Ján Poisson Marková, Simona Plzák, Jan Kluh, Jan Seeman, Pavel Producer: 20200218 In: European archives of oto-rhino-laryngology : official journal of the European Federation of Oto-Rhino-Laryngological Societies (EUFOS) : affiliated with the German Society for Oto-Rhino-Laryngology - Head and Neck Surgery vol. 276 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)