Publications by authors named "Jessica Bos"

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DISP1 deficiency: Monoallelic and biallelic variants cause a spectrum of midline craniofacial malformations.
Alinoë Lavillaureix, Paul Rollier, Artem Kim, Veranika Panasenkava, Marie De Tayrac, Jessica Bos

Genet Med· July 2024

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Vascular Ehlers-Danlos Syndrome: A Comprehensive Natural History Study in a Dutch National Cohort of 142 Patients.
Serwet Demirdas, Lisa M van den Bersselaar, Rosan Lechner, Jessica Bos, Suzanne I M Alsters

Circ Genom Precis Med· June 2024

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Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood.
Michael A Levy, David B Beck, Kay Metcalfe, Sofia Douzgou, Sivagamy Sithambaram, Jessica Bos

NPJ Genom Med· November 2021

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Author Correction: Deficiency of TET3 leads to a genome-wide DNA hypermethylation episignature in human whole blood.
Michael A Levy, David B Beck, Kay Metcalfe, Sofia Douzgou, Sivagamy Sithambaram, Jessica Bos

NPJ Genom Med· November 2021

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