University of Strasbourg-ko ikertzaileekin lankidetzan egindako argitalpenak (4)

2016

  1. Uncommon nucleotide excision repair phenotypes revealed by targeted high-throughput sequencing

    Orphanet Journal of Rare Diseases, Vol. 11, Núm. 1

2010

  1. Mutation update for the CSB/ERCC6 and CSA/ERCC8 genes involved in Cockayne syndrome

    Human Mutation, Vol. 31, Núm. 2, pp. 113-126

2005

  1. Trends and geographic inequalities in the prevalence of Down syndrome in Europe, 1980-1999

    Revue d'Epidemiologie et de Sante Publique

2004

  1. Prenatal diagnostic procedures used in pregnancies with congenital malformations in 14 regions of Europe

    Prenatal Diagnosis, Vol. 24, Núm. 11, pp. 908-912