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Identification of an episignature for CHD3-related Snijders Blok-Campeau syndrome reveals heterogeneity in the CHARGE syndrome episignature: towards a better characterisation of chromatinopathies

Amandine Santini et al.
HAL (France) · Papers · License: Open Access
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dna-methylationrare-diseases
Rare Diseases, Snijders Blok-Campeau syndrome, DNA methylation, 0, Episignature, CHD3
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Record · ID 254296
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