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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
Blondeel, E., Molina-Gomes, D., Bouhanna, P., Fauvert, D., Crosnier, H., Dessuant, H., Vialard, F.Volume:
2
Language:
english
Journal:
Clinical Case Reports
DOI:
10.1002/ccr3.71
Date:
June, 2014
File:
PDF, 593 KB
english, 2014