ŠERÝ, Omar, Ondřej BONCZEK, Alena HLOUŠKOVÁ, Pavlína ČERNOCHOVÁ, Jiří VANĚK, Ivan MÍŠEK, Přemysl KREJČÍ and Lydie IZAKOVIČOVÁ HOLLÁ. A screen of a large Czech cohort of oligodontia patients implicates a novel mutation in the PAX9 gene. EUROPEAN JOURNAL OF ORAL SCIENCES. Blackwell, vol. 123, No 2, p. 65-71. ISSN 0909-8836. doi:10.1111/eos.12170. 2015.
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Basic information
Original name A screen of a large Czech cohort of oligodontia patients implicates a novel mutation in the PAX9 gene
Name in Czech Screening velké české kohorty pacientů s oligodoncií prokázal novou mutaci v genu pro PAX9
Authors ŠERÝ, Omar (203 Czech Republic, guarantor, belonging to the institution), Ondřej BONCZEK (203 Czech Republic, belonging to the institution), Alena HLOUŠKOVÁ (203 Czech Republic, belonging to the institution), Pavlína ČERNOCHOVÁ (203 Czech Republic, belonging to the institution), Jiří VANĚK (203 Czech Republic, belonging to the institution), Ivan MÍŠEK (203 Czech Republic, belonging to the institution), Přemysl KREJČÍ (203 Czech Republic) and Lydie IZAKOVIČOVÁ HOLLÁ (203 Czech Republic, belonging to the institution).
Edition EUROPEAN JOURNAL OF ORAL SCIENCES, Blackwell, 2015, 0909-8836.
Other information
Original language English
Type of outcome Article in a journal
Field of Study 30200 3.2 Clinical medicine
Country of publisher United States of America
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 1.607
RIV identification code RIV/00216224:14310/15:00080625
Organization unit Faculty of Science
Doi http://dx.doi.org/10.1111/eos.12170
UT WoS 000351166700002
Keywords (in Czech) PAX9; ageneze zubů; oligodoncie; jednovaječná dvojčata; mutační screening
Keywords in English PAX9; tooth agenesis; oligodontia; monozygotic twins; mutation screening
Tags AKR, EL OK, podil, rivok
Changed by Changed by: Ing. Andrea Mikešková, učo 137293. Changed: 24/3/2016 10:03.
Abstract
The aim of the present study was to perform screening for mutations and/or polymorphisms in the critical regions of PAX9 and MSX1 genes in a group of 270 patients with tooth agenesis and in 30 healthy subjects of the Czech origin.
Abstract (in Czech)
Cílem této práce bylo provedení screeningu mutací a/nebo polymorfizmů v kritických oblastech PAX9 a MSX1 genů u skupiny 270 pacientů s agenezí zubů a 30 zdravých kontrol v české populaci.
Links
GB14-37368G, research and development projectName: Centrum orofaciálního vývoje a regenerace
Investor: Czech Science Foundation
NT11420, research and development projectName: Molekulární diagnostika hypodoncie a možnosti zubních autotransplantací
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