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	21.	A novel insertion of a rearranged L1 element in exon 44 of the dystrophin gene: further evidence for possible bias in retroposon integration. [electronic resource] by Musova, Zuzana Hedvicakova, Petra Mohrmann, Marketa Tesarova, Marketa Krepelova, Anna Zeman, Jiri Sedlacek, Zdenek Producer: 20060913 In: Biochemical and biophysical research communications vol. 347 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	22.	Molecular genetic analysis of 103 sporadic colorectal tumours in Czech patients. [electronic resource] by Vasovcak, Peter Pavlikova, Kristyna Sedlacek, Zdenek Skapa, Petr Kouda, Martin Hoch, Jiri Krepelova, Anna Producer: 20120413 In: PloS one vol. 6 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	23.	FMR1 gene expansion, large deletion of Xp, and skewed X-inactivation in a girl with mental retardation and autism. [electronic resource] by Vazna, Alzbeta Musova, Zuzana Vlckova, Marketa Novotna, Dhahuse Dvorakova, Lenka Hrdlicka, Michal Havlovicova, Marketa Sedlacek, Zdenek Producer: 20100812 In: American journal of medical genetics. Part A vol. 152A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	24.	A girl with neurofibromatosis type 1, atypical autism and mosaic ring chromosome 17. [electronic resource] by Havlovicova, Marketa Novotna, Drahuse Kocarek, Eduard Novotna, Kamila Bendova, Sarka Petrak, Borivoj Hrdlicka, Michal Sedlacek, Zdenek Producer: 20070326 In: American journal of medical genetics. Part A vol. 143A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	25.	TP53 gene mutations are rare in nondysplastic Barrett's esophagus. [electronic resource] by Novotna, Kamila Trkova, Marie Pazdro, Alexandr Smejkal, Milan Soukupova, Alzbeta Kodetova, Daniela Smejkal, Premysl Sedlacek, Zdenek Producer: 20060207 In: Digestive diseases and sciences vol. 51 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	26.	Analysis of genetic events in 17p13 and 9p21 regions supports predominant monoclonal origin of multifocal and recurrent bladder cancer. [electronic resource] by Trkova, Marie Babjuk, Marko Duskova, Jaroslava Benesova-Minarikova, Lucie Soukup, Viktor Mares, Jaroslav Minarik, Marek Sedlacek, Zdenek Producer: 20061208 In: Cancer letters vol. 242 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	27.	Monozygotic twins with 17q21.31 microdeletion syndrome. [electronic resource] by Vlckova, Marketa Hancarova, Miroslava Drabova, Jana Slamova, Zuzana Koudova, Monika Alanova, Renata Mannik, Katrin Kurg, Ants Sedlacek, Zdenek Producer: 20141121 In: Twin research and human genetics : the official journal of the International Society for Twin Studies vol. 17 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	28.	Expanded [electronic resource] by Musova, Zuzana Hancarova, Miroslava Havlovicova, Marketa Pourova, Radka Hrdlicka, Michal Kraus, Josef Trkova, Marie Stejskal, David Sedlacek, Zdenek Publication details: Neuropsychiatric disease and treatment 2016 In: Neuropsychiatric disease and treatment vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	29.	Long term follow-up in a patient with a de novo microdeletion of 14q11.2 involving CHD8. [electronic resource] by Drabova, Jana Seemanova, Eva Hancarova, Miroslava Pourova, Radka Horacek, Martin Jancuskova, Tereza Pekova, Sona Novotna, Drahuse Sedlacek, Zdenek Producer: 20151214 In: American journal of medical genetics. Part A vol. 167A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	30.	A novel variant of C12orf4 in a consanguineous Armenian family confirms the etiology of autosomal recessive intellectual disability type 66 with delineation of the phenotype. [electronic resource] by Hancarova, Miroslava Babikyan, Davit Bendova, Sarka Midyan, Susanna Prchalova, Darina Shahsuvaryan, Gohar Stranecky, Viktor Sarkisian, Tamara Sedlacek, Zdenek Producer: 20200619 In: Molecular genetics & genomic medicine vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	31.	Not EEG abnormalities but epilepsy is associated with autistic regression and mental functioning in childhood autism. [electronic resource] by Hrdlicka, Michal Komarek, Vladimir Propper, Lukas Kulisek, Robert Zumrova, Alena Faladova, Ludvika Havlovicova, Marketa Sedlacek, Zdenek Blatny, Marek Urbanek, Tomas Producer: 20050104 In: European child & adolescent psychiatry vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	32.	Array comparative genome hybridization in patients with developmental delay: two example cases. [electronic resource] by Hancarova, Miroslava Drabova, Jana Zmitkova, Zuzana Vlckova, Marketa Hedvicakova, Petra Novotna, Drahuse Vlckova, Zdenka Vejvalkova, Sarka Marikova, Tatana Sedlacek, Zdenek Producer: 20120525 In: New biotechnology vol. 29 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	33.	A patient showing features of both SBBYSS and GPS supports the concept of a KAT6B-related disease spectrum, with mutations in mid-exon 18 possibly leading to combined phenotypes. [electronic resource] by Vlckova, Marketa Simandlova, Martina Zimmermann, Pavel Stranecky, Viktor Hartmannova, Hana Hodanova, Katerina Havlovicova, Marketa Hancarova, Miroslava Kmoch, Stanislav Sedlacek, Zdenek Producer: 20160819 In: European journal of medical genetics vol. 58 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	34.	Spinocerebellar ataxias type 8, 12, and 17 and dentatorubro-pallidoluysian atrophy in Czech ataxic patients. [electronic resource] by Musova, Zuzana Sedlacek, Zdenek Mazanec, Radim Klempir, Jiri Roth, Jan Plevova, Pavlina Vyhnalek, Martin Kopeckova, Marta Apltova, Ludmila Krepelova, Anna Zumrova, Alena Producer: 20130905 In: Cerebellum (London, England) vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	35.	A novel frameshift mutation in the AFG3L2 gene in a patient with spinocerebellar ataxia. [electronic resource] by Musova, Zuzana Kaiserova, Michaela Kriegova, Eva Fillerova, Regina Vasovcak, Peter Santava, Alena Mensikova, Katerina Zumrova, Alena Krepelova, Anna Sedlacek, Zdenek Kanovsky, Petr Producer: 20141222 In: Cerebellum (London, England) vol. 13 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	36.	Molecular Cytogenetic Diagnostics of Marker Chromosomes: Analysis in Four Prenatal Cases and Long-Term Clinical Evaluation of Carriers. [electronic resource] by Tesner, Pavel Vlckova, Marketa Drabova, Jana Vseticka, Jan Klimova, Anna Lastuvkova, Jana Zidovska, Jana Kremlikova Pourova, Radka Hancarova, Miroslava Sedlacek, Zdenek Kocarek, Eduard Producer: 20180724 In: Cytogenetic and genome research vol. 154 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	37.	Subtypes of autism by cluster analysis based on structural MRI data. [electronic resource] by Hrdlicka, Michal Dudova, Iva Beranova, Irena Lisy, Jiri Belsan, Tomas Neuwirth, Jiri Komarek, Vladimir Faladova, Ludvika Havlovicova, Marketa Sedlacek, Zdenek Blatny, Marek Urbanek, Tomas Producer: 20051021 In: European child & adolescent psychiatry vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	38.	Highly unstable sequence interruptions of the CTG repeat in the myotonic dystrophy gene. [electronic resource] by Musova, Zuzana Mazanec, Radim Krepelova, Anna Ehler, Edvard Vales, Jiri Jaklova, Radka Prochazka, Tomas Koukal, Petr Marikova, Tatana Kraus, Josef Havlovicova, Marketa Sedlacek, Zdenek Producer: 20090923 In: American journal of medical genetics. Part A vol. 149A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	39.	A boy with developmental delay and mosaic supernumerary inv dup(5)(p15.33p15.1) leading to distal 5p tetrasomy - case report and review of the literature. [electronic resource] by Tesner, Pavel Drabova, Jana Stolfa, Miroslav Kudr, Martin Kyncl, Martin Moslerova, Veronika Novotna, Drahuse Kremlikova Pourova, Radka Kocarek, Eduard Rasplickova, Tereza Sedlacek, Zdenek Vlckova, Marketa Publication details: Molecular cytogenetics 2018 In: Molecular cytogenetics vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	40.	Very short DNA segments can be detected and handled by the repair machinery during germline chromothriptic chromosome reassembly. [electronic resource] by Slamova, Zuzana Nazaryan-Petersen, Lusine Mehrjouy, Mana M Drabova, Jana Hancarova, Miroslava Marikova, Tatana Novotna, Drahuse Vlckova, Marketa Vlckova, Zdenka Bak, Mads Zemanova, Zuzana Tommerup, Niels Sedlacek, Zdenek Producer: 20190513 In: Human mutation vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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