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
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F. Vialard | P. Bouhanna | H. Crosnier | D. Fauvert | H. Dessuant | D. Molina‐Gomes | Eléonore Blondeel