Publications by authors named "R Behulova"

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Case Report: The Role of Molecular Analysis of the Gene in Asymptomatic Individuals.
Katarína Fabišíková, Olívia Hamidová, Regína Lohajová Behulová, Katarína Závodná, Petra Priščáková

Front Genet· December 2020

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Molecular biomarkers in the diagnostic of patients with colorectal cancer.
Katarína Fabišíková, Regina Lohajová Behulová, Vanda Repiska

Neuro Endocrinol Lett· December 2019

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Founder mutations in NDRG1 and HK1 genes are common causes of inherited neuropathies among Roma/Gypsies in Slovakia.
Dana Gabrikova, Martin Mistrik, Jarmila Bernasovska, Alexandra Bozikova, Regina Behulova

J Appl Genet· November 2013

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The frequency of factor V Leiden and prothrombin G20210A mutations in Slovak and Roma (Gypsy) ethnic group of Eastern Slovakia.
Alexandra Bôžiková, Dana Gabriková, Adriana Sovičová, Regina Behulová, Soňa Mačeková

J Thromb Thrombolysis· October 2012

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Unique frequencies of HFE gene variants in Roma/Gypsies.
Dana Gabriková, Jarmila Bernasovská, Soňa Mačeková, Alexandra Bôžiková, Ivan Bernasovský

J Appl Genet· May 2012

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