Emílie Vyhnálková

1PUBLICATIONS
7CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)
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Publications (1)

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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.

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Frequent Collaborators

1 joint publications

Júlia Martinková

1 joint publications

Martin Schwarz

1 joint publications

Miroslava Balaščaková

1 joint publications

Veronika Biddle

1 joint publications

Lenka Fajkusová

1 joint publications

Lukáš Ryba

1 joint publications

Anna Křepelová

Frequent Collaborators

1 joint publications

Júlia Martinková

1 joint publications

Martin Schwarz

1 joint publications

Miroslava Balaščaková

1 joint publications

Veronika Biddle

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