Suchergebnisse
Suchergebnisse:
The myCeGaT Portal provides access to genetic testing results and reports for patients and healthcare professionals.
myCeGaT Portal
GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel Blockers.
Mutations in the gene PDE6C encoding the catalytic subunit of the cone photoreceptor phosphodiesterase in patients with achromatopsia.
العربية Arabisch ar; Dansk Dänisch da; English_GB Englisch_GB en_GB
العربية Arabisch ar; Dansk Dänisch da; English_GB Englisch_GB en_GB
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