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	1.	Deletions of 9q21.3 including NTRK2 are associated with severe phenotype. [electronic resource] by Hancarova, Miroslava Puchmajerova, Alena Drabova, Jana Karaskova, Eliska Vlckova, Marketa Sedlacek, Zdenek Producer: 20150521 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)
	2.	Analysis of 31-year-old patient with SYNGAP1 gene defect points to importance of variants in broader splice regions and reveals developmental trajectory of SYNGAP1-associated phenotype: case report. [electronic resource] by Prchalova, Darina Havlovicova, Marketa Sterbova, Katalin Stranecky, Viktor Hancarova, Miroslava Sedlacek, Zdenek Producer: 20170803 In: BMC medical genetics vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Association of 17q24.2-q24.3 deletions with recognizable phenotype and short telomeres. [electronic resource] by Hancarova, Miroslava Malikova, Marcela Kotrova, Michaela Drabova, Jana Trkova, Marie Sedlacek, Zdenek Producer: 20190521 In: American journal of medical genetics. Part A vol. 176 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	A patient with de novo 0.45 Mb deletion of 2p16.1: the role of BCL11A, PAPOLG, REL, and FLJ16341 in the 2p15-p16.1 microdeletion syndrome. [electronic resource] by Hancarova, Miroslava Simandlova, Martina Drabova, Jana Mannik, Katrin Kurg, Ants Sedlacek, Zdenek Producer: 20130909 In: American journal of medical genetics. Part A vol. 161A Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	Hypophosphatasia due to uniparental disomy. [electronic resource] by Hancarova, Miroslava Krepelova, Anna Puchmajerova, Alena Soucek, Ondrej Prchalova, Darina Sumnik, Zdenek Sedlacek, Zdenek Producer: 20160209 In: Bone vol. 81 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	6.	A high frequency of the Cystic Fibrosis 2184insA mutation in Western Ukraine: genotype-phenotype correlations, relevance for newborn screening and genetic testing. [electronic resource] by Makukh, Halyna Krenková, Petra Tyrkus, Marta Bober, Lyudmyla Hancárová, Miroslava Hnateyko, Oleh Macek, Milan Producer: 20110131 In: Journal of cystic fibrosis : official journal of the European Cystic Fibrosis Society vol. 9 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Identification of a patient with intellectual disability and de novo 3.7 Mb deletion supports the existence of a novel microdeletion syndrome in 2p14-p15. [electronic resource] by Hancarova, Miroslava Vejvalkova, Sarka Trkova, Marie Drabova, Jana Dleskova, Alzbeta Vlckova, Marketa Sedlacek, Zdenek Producer: 20130325 In: Gene vol. 516 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	A 15 Mb large paracentric chromosome 21 inversion identified in Czech population through a pair of flanking duplications. [electronic resource] by Drabova, Jana Trkova, Marie Hancarova, Miroslava Novotna, Drahuse Hejtmankova, Michaela Havlovicova, Marketa Sedlacek, Zdenek Producer: 20141121 In: Molecular cytogenetics vol. 7 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	9.	Parental gonadal but not somatic mosaicism leading to de novo NFIX variants shared by two brothers with Malan syndrome. [electronic resource] by Hancarova, Miroslava Havlovicova, Marketa Putzova, Martina Vseticka, Jan Prchalova, Darina Stranecky, Viktor Sedlacek, Zdenek Producer: 20200803 In: American journal of medical genetics. Part A vol. 179 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Chromosome 12q13.13 deletions involving the HOXC gene cluster: phenotype and candidate genes. [electronic resource] by Hancarova, Miroslava Simandlova, Martina Drabova, Jana Petrak, Borivoj Koudova, Monika Havlovicova, Marketa Sedlacek, Zdenek Producer: 20130812 In: European journal of medical genetics vol. 56 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Cell-free fetal DNA in maternal plasma during physiological single male pregnancies: methodology issues and kinetics. [electronic resource] by Horinek, Ales Korabecna, Marie Panczak, Ales Ulcova Gallova, Zdenka Nouzova, Kamila Calda, Pavel Hancarova, Miroslava Producer: 20080918 In: Fetal diagnosis and therapy vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	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)
	13.	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)
	14.	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)
	15.	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)
	16.	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)
	17.	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)
	18.	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)
	19.	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)
	20.	HCFC1 loss-of-function mutations disrupt neuronal and neural progenitor cells of the developing brain. [electronic resource] by Jolly, Lachlan A Nguyen, Lam Son Domingo, Deepti Sun, Ying Barry, Simon Hancarova, Miroslava Plevova, Pavlina Vlckova, Marketa Havlovicova, Marketa Kalscheuer, Vera M Graziano, Claudio Pippucci, Tommaso Bonora, Elena Sedlacek, Zdenek Gecz, Jozef Producer: 20160204 In: Human molecular genetics vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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