Submicroscopic deletions at 13q32.1 cause congenital microcoria
Am J Hum Genet. 2015 Apr 2 Authors Fares-Taie L, Gerber S, Tawara A, Ramirez-Miranda A, Douet JY, Verdin H, Guilloux A, Zenteno JC, Kondo H, Moisset H, Passet B, Yamamoto K,Iwai M, Tanaka T, Nakamura Y, Kimura W, Bole-Feysot C, Vilotte […]
Molecular investigations, CGH-Array, Molecular karyotype, Postnatal diagnosis, Congenital microcoria, Publication