Refinement of Genotype-Phenotype Correlation in 18 Patients Carrying a 1q24q25 Deletion

Chatron, N.; Haddad, V.; Andrieux, J.; Desir, J.; Boute, O.; Dieux, A.; ... ; Schluth-Bolard, C. (2015)

Article / Letter to editor

• 1q24q25 deletion
• DNM3
• growth retardation
• brachydactyly
• intellectual disability

• All authors: Chatron, N.; Haddad, V.; Andrieux, J.; Desir, J.; Boute, O.; Dieux, A.; Baumann, C.; Drunat, S.; Gerard, M.; Bonnet, C.; Leheup, B.; Till, M.; Rossi, M.; Flori, E.; Alembik, Y.; Stewart, H.; McParland, J.; Bernardini, L.; Castelluccio, P.; Roos, L.; Tumer, Z.; Fagan, K.; Hackett, A.; Bain, N.; Haeringen, A. van; Ruivenkamp, C.; Benzacken, B.; Sanlaville, D.; Edery, P.; Aboura, A.; Schluth-Bolard, C.
• Date: 2015-05-31
• Journal: American Journal of Medical Genetics Part A
• Volume: 167
• Issue: 5
• Pages: 1008 - 1017
• DOI: doi:10.1002/ajmg.a.36856