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 2014

Prenatal diagnosis of recurrent hypoplastic left heart syndrome associated with MYH6 variants: a case report

por Najib, B., Quibel, T., Tessier, A., Mortreux, J., Bouvagnet, P., Cohen, C., Vialard, F., Dard, R.
Publicado 2023

To be or not to be [fertile], that is the question

por Swierkowski-Blanchard, N., Alter, L., Salama, S., Muratorio, C., Bergere, M., Jaoul, M., Vialard, F., Bailly, M., Selva, J., Boitrelle, F.
Publicado 2016

Whole-exome sequencing in patients with maturation arrest: a potential additional diagnostic tool for prevention of recurrent negative testicular sperm extraction outcomes

por Ghieh, F, Barbotin, A L, Swierkowski-Blanchard, N, Leroy, C, Fortemps, J, Gerault, C, Hue, C, Mambu Mambueni, H, Jaillard, S, Albert, M, Bailly, M, Izard, V, Molina-Gomes, D, Marcelli, F, Prasivoravong, J, Serazin, V, Dieudonne, M N, Delcroix, M, Garchon, H J, Louboutin, A, Mandon-Pepin, B, Ferlicot, S, Vialard, F
Publicado 2022