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VENCESLÁ, A., BAENA, M., FARES TAIE, L., CORNET, M., BAIGET, M., TIZZANO, E. F.
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Implication of non-coding PAX6 mutations in aniridia
Plaisancié, Julie, Tarilonte, M., Ramos, P., Jeanton-Scaramouche, C., Gaston, V., Dollfus, H., Aguilera, D., Kaplan, J., Fares-Taie, L., Blanco-Kelly, F., Villaverde, C., Francannet, C., Goldenberg, A., Arroyo, I., Rozet, J. M., Ayuso, C., Chassaing, N., Calvas, P., Corton, M.
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Published in Acta ophthalmologica (Oxford, England) (01.10.2016)
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Published in Acta ophthalmologica (Oxford, England) (01.10.2016)
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Abnormal respiratory cilia in non-syndromic Leber congenital amaurosis with CEP290 mutations
Papon, J F, Perrault, I, Coste, A, Louis, B, Gérard, X, Hanein, S, Fares-Taie, L, Gerber, S, Defoort-Dhellemmes, S, Vojtek, A M, Kaplan, J, Rozet, J M, Escudier, E
Published in Journal of medical genetics (01.12.2010)
Published in Journal of medical genetics (01.12.2010)
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Impact of socio-economic status on the prevalence of severe hypertriglyceridemia in Argentina
Corral, P., Sáenz, B., Blautzik, F., Taie, L. Fares, Larrieu, L. Rosa, Bilbao, M., Sayanes, M., Matta, M.
Published in Atherosclerosis (01.08.2023)
Published in Atherosclerosis (01.08.2023)
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Is the modification of the 13q32.1 regulatory landscape the cause of congenital microcoria?
Published in Acta ophthalmologica (Oxford, England)
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