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G Madsen

Showing results (141-150 of 143) with videos related to

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Nature Communications|January 13, 2026
Biallelic variants in CELSR1 cause brain malformations, neurodevelopmental disorders and epilepsy in humansClaudia M Bonardi, Rikke S Møller, Nuria Ruiz-Reig, et al.
Brain : a Journal of Neurology|April 16, 2020
Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of functionMonica Zilmer, Andrew C Edmondson, Sumeet A Khetarpal, et al.
Nature Communications|May 12, 2021
Elp2 mutations perturb the epitranscriptome and lead to a complex neurodevelopmental phenotypeMarija Kojic, Tomasz Gawda, Monika Gaik, et al.
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Showing results (141-150 of 143) with videos related to

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Pageof 15
You have reached the last page of results.This site can display upto 143 results.
Nature Communications|January 13, 2026
Biallelic variants in CELSR1 cause brain malformations, neurodevelopmental disorders and epilepsy in humansClaudia M Bonardi, Rikke S Møller, Nuria Ruiz-Reig, et al.
Brain : a Journal of Neurology|April 16, 2020
Novel congenital disorder of O-linked glycosylation caused by GALNT2 loss of functionMonica Zilmer, Andrew C Edmondson, Sumeet A Khetarpal, et al.
Nature Communications|May 12, 2021
Elp2 mutations perturb the epitranscriptome and lead to a complex neurodevelopmental phenotypeMarija Kojic, Tomasz Gawda, Monika Gaik, et al.
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