Anna Křepelová

2PUBLICATIONS
13CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Cancer genetics
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Publications (2)

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|Jun 04, 2026
A c.89G>C p.(Gly30Ala) Variant in the DHCR7 Gene as a Cause of a Mild Phenotype in the Smith-Lemli-Opitz Syndrome.

|Mar 08, 2024
Functional studies associate novel DUOX2 gene variants detected in heterozygosity to Crohn's disease.

Martin Schwarz, Matej Gazdarica, Eva Froňková

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Martin Schwarz

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Matej Gazdarica

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Eva Froňková

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Michael Svatoň

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Jiří Bronský

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Markéta Havlovicová

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Milan Macek

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Júlia Martinková

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Emílie Vyhnálková

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Miroslava Balaščaková

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Martin Schwarz

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Matej Gazdarica

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Eva Froňková

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Michael Svatoň

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