Search Results - Vélez Rengifo, G J

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    CTNNB1 gene mutation associated with neurodevelopmental disorder, microcephaly, and persistence of bilateral hyperplastic primary vitreous: A case report and literature review

    CTNNB1 gene mutation associated with neurodevelopmental disorder, microcephaly, and persistence of bilateral hyperplastic primary vitreous: A case report and literature review by Zuluaga Gómez, L.M., Caballero Mojica, S.C., Vélez Rengifo, G.J., Bravo Acosta, J.D., Montoya Villada, J.H.

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    CTNNB1 gene mutation associated with neurodevelopmental disorder, microcephaly, and persistence of bilateral hyperplastic primary vítreous: a case report and literature review

    CTNNB1 gene mutation associated with neurodevelopmental disorder, microcephaly, and persistence of bilateral hyperplastic primary vítreous: a case report and literature review by Zuluaga Gómez, L M, Caballero Mojica, S C, Vélez Rengifo, G J, Bravo Acosta, J D, Montoya Villada, J H

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    CTNNB1 gene mutation associated with neurodevelopmental disorder, microcephaly, and persistence of bilateral hyperplastic primary vítreous: a case report and literature review

    CTNNB1 gene mutation associated with neurodevelopmental disorder, microcephaly, and persistence of bilateral hyperplastic primary vítreous: a case report and literature review by Zuluaga Gómez, L M, Caballero Mojica, S C, Vélez Rengifo, G J, Bravo Acosta, J D, Montoya Villada, J H

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