Birth of a boy with isolated short stature after prenatal diagnosis of a Xp22.3 nullosomy due to an inherited t(X;15) (p22.3;p10) translocation

Por Blondeel, E, Molina-Gomes, D, Bouhanna, P, Fauvert, D, Crosnier, H, Dessuant, H, Vialard, F
Publicado em 2014