Chiara Conte
Rome, Italy
Last Updated: 09/26/2026
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Found 8 publications
Prenatal diagnosis of Cockayne syndrome type A based on the identification of two novel mutations in the ERCC8 gene.
Journal: Genetic testing and molecular biomarkers
Published: March 25, 2009
Gene symbol: ED1. Disease: X-linked anhidrotic ectodermal dysplasia.
Journal: Human genetics
Published: April 04, 2008
Showing 1-8 of 8
Last Updated: 09/26/2026