Miroslava Balaščáková

2PUBLICATIONS
25CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Gene mapping
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Publications (2)

|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.

|May 20, 2020
Expanding the phenotype spectrum associated with pathogenic variants in the COL2A1 and COL11A1 genes.

Jana Čopíková, Jana Paděrová, Věra Románková

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Frequent Collaborators

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Jana Čopíková

1 joint publications

Jana Paděrová

1 joint publications

Věra Románková

1 joint publications

Markéta Havlovicová