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Page 1
[Cat eye syndrome].
Bremond-Gignac D, Morin G, Jedraszak G, Receveur A, Rochette J, Copin H. Bremond-Gignac D, et al. Among authors: copin h. J Fr Ophtalmol. 2015 Apr;38(4):368-9. doi: 10.1016/j.jfo.2014.09.016. Epub 2015 Mar 20. J Fr Ophtalmol. 2015. PMID: 25799388 French. No abstract available.
A severe prenatal presentation of Cat Eye Syndrome.
Jedraszak G, Receveur A, Andrieux J, Naepels P, Mathieu-Dramard M, Bremond-Gignac D, Sevestre H, Copin H, Rochette J. Jedraszak G, et al. Among authors: copin h. Clin Dysmorphol. 2013 Oct;22(4):175-177. doi: 10.1097/MCD.0000000000000011. Clin Dysmorphol. 2013. PMID: 23982124 No abstract available.
[WAGR Syndrome].
Brémond-Gignac D, Copin H. Brémond-Gignac D, et al. Among authors: copin h. J Fr Ophtalmol. 2004 Dec;27(10):1198-9. doi: 10.1016/s0181-5512(04)96295-x. J Fr Ophtalmol. 2004. PMID: 15687936 French. No abstract available.
Clinical and molecular characterization of the 20q11.2 microdeletion syndrome: six new patients.
Jedraszak G, Demeer B, Mathieu-Dramard M, Andrieux J, Receveur A, Weber A, Maye U, Foulds N, Temple IK, Crolla J, Alex-Cordier MP, Sanlaville D, Ewans L, Wilson M, Armstrong R, Clarkson A, Copin H, Morin G. Jedraszak G, et al. Among authors: copin h. Am J Med Genet A. 2015 Mar;167A(3):504-11. doi: 10.1002/ajmg.a.36882. Epub 2015 Jan 8. Am J Med Genet A. 2015. PMID: 25572454 Review.
[Groenouw type II macular corneal dystrophy: case report].
Cretu I, Brémond-Gignac D, Milazzo S, Jany B, Ikoli JF, Copin H, Sevestre H. Cretu I, et al. Among authors: copin h. J Fr Ophtalmol. 2012 Dec;35(10):786-91. doi: 10.1016/j.jfo.2011.11.014. Epub 2012 Sep 29. J Fr Ophtalmol. 2012. PMID: 23026701 French.
98 results