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1887
107506
Refinement of Genotype-Phenotype Correlation in 18 Patients Carrying a 1q24q25 Deletion
Author(s):
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.
Published
2015
Publication type
Article / Letter to editor
1q24q25 deletion
DNM3
growth retardation
brachydactyly
intellectual disability
Date issued
2015-05-31
Language
English
Is part of
American Journal of Medical Genetics Part A (2015), Vol. 167, no. 5, p. 1008-1017
hdl
1887/107506
doi
10.1002/ajmg.a.36856
Persistent identifier url
https://hdl.handle.net/1887/107506
Metadata only