Věra Kebrdlová

SHOX gene defects and selected dysmorphic signs in patients of idiopathic short stature and Léri–Weill dyschondrosteosis

Kateřina Hirschfeldová, Roman Šolc, A Baxová et al. · Gene · 2011 · 49 citations

Mendelian Disorder, Genetic Disorder, Genetics +7

The S18Y polymorphism in the UCHL1 gene is a genetic modifier in Huntington’s disease

Silke Metzger, Peter Bauer, Juergen Tomiuk et al. · Neurogenetics · 2005 · 47 citations · Full text

Genetic Disorder, Genetics, Human Polymorphism +7

Application of the new insertion–deletion polymorphism kit for forensic identification and parentage testing on the Czech population

Anastassiya Zidkova, Aleš Hořínek, Věra Kebrdlová et al. · International Journal of Legal Medicine · 2011 · 44 citations · Full text

Genetic Testing, Genetics, Genetic Epidemiology +24

Genetic analysis of candidate genes modifying the age-at-onset in Huntington’s disease

Silke Metzger, Peter Bauer, Jürgen Tomiuk et al. · Human Genetics · 2006 · 41 citations

Genetic Analysis, Neurodegenerative Diseases, Candidate Genes +11

Molecular analysis of the<i>APC</i>and<i>MYH</i>genes in Czech families affected by FAP or multiple adenomas: 13 novel mutations

Jana Vandrovcová, Jitka Štekrová, Věra Kebrdlová et al. · Human Mutation · 2004 · 35 citations · Full text