Jitka Štekrová

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

Genotype–phenotype correlation in children with autosomal dominant polycystic kidney disease

Filip Fencl, J Janda, Květa Bláhová et al. · Pediatric Nephrology · 2009 · 39 citations

Genetic Disorder, Medicine, Genetics +12

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

Autosomal dominant polycystic kidney disease in a family with mosaicism and hypomorphic allele

Jana Reiterová, Jitka Štekrová, M Merta et al. · BMC Nephrology · 2013 · 33 citations · Full text

Novel APC mutations in Czech and Slovak FAP families: clinical and genetic aspects

Jitka Štekrová, Martina Sulova, Věra Kebrdlová et al. · BMC Medical Genetics · 2007 · 28 citations · Full text