Publications by authors named "Simona Poisson Markova"

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Spectrum and frequencies of non GJB2 gene mutations in Czech patients with early non-syndromic hearing loss detected by gene panel NGS and whole-exome sequencing.
Dana Safka Brozkova, Simona Poisson Marková, Anna Uhrová Mészárosová, Ján Jenčík, Vlasta Čejnová

Clin Genet· December 2020

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Moderate sensorineural hearing loss is typical for DFNB16 caused by various types of mutations affecting the STRC gene.
Zdeněk Čada, Dana Šafka Brožková, Zuzana Balatková, Pavlína Plevová, Dagmar Rašková

Eur Arch Otorhinolaryngol· December 2019

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Genome-wide uniparental diploidy of all paternal chromosomes in an 11-year-old girl with deafness and without malignancy.
Irena Borgulová, Inna Soldatova, Martina Putzová, Marcela Malíková, Jana Neupauerová

J Hum Genet· July 2018

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STRC Gene Mutations, Mainly Large Deletions, are a Very Important Cause of Early-Onset Hereditary Hearing Loss in the Czech Population.
Simona Poisson Marková, Dana Šafka Brožková, Petra Laššuthová, Anna Mészárosová, Marcela Krůtová

Genet Test Mol Biomarkers· February 2018

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