Search Results - Quiezi, Rodrigo G.

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    Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies

    Exclusion of mutations in TGIF, ALX3, and ALX4 genes in patients with the syndrome of frontonasal dysgenesis, callosal agenesis, basal encephalocele, and eye anomalies by Ribeiro-Bicudo, Lucilene Arilho, Quiezi, Rodrigo G., Guion-Almeida, Maria Leine, Legnaro, Chiara, Richieri-Costa, Antonio

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