HOŘÍNOVÁ, Věra, Vladimíra VRANOVÁ, Petr KUGLÍK, Alexandra OLTOVÁ and Petr HOŘÍN. Clinical characterization of a microdeletion syndrome in Xq22.3 in a Czech family. In European Human Genetics Conference. 2009. ISSN 1018-4813.
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Basic information
Original name Clinical characterization of a microdeletion syndrome in Xq22.3 in a Czech family
Name in Czech Klinická charakterizace mikrodelečního syndromu Xq22.3 u české rodiny
Authors HOŘÍNOVÁ, Věra, Vladimíra VRANOVÁ, Petr KUGLÍK, Alexandra OLTOVÁ and Petr HOŘÍN.
Edition European Human Genetics Conference, 2009.
Other information
Original language English
Type of outcome Conference abstract
Field of Study Genetics and molecular biology
Country of publisher Czech Republic
Confidentiality degree is not subject to a state or trade secret
Impact factor Impact factor: 3.564
Organization unit Faculty of Science
ISSN 1018-4813
Changed by Changed by: RNDr. Vladimíra Vallová, Ph.D., učo 108411. Changed: 28/4/2011 13:40.
Links
MSM0021622415, plan (intention)Name: Molekulární podstata buněčných a tkáňových regulací
Investor: Ministry of Education, Youth and Sports of the CR, Molecular basis of cell and tissue regulations
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