Search Results - Aguiar, Marcos J. Burle de

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  1. 1
    Uncommon Oral Cleft in Wolf-Hirschhorn Syndrome

    Uncommon Oral Cleft in Wolf-Hirschhorn Syndrome by Aquino, Sibele Nascimento de, Machado, Renato A., Paranaíba, Lívia Maris R., Coletta, Ricardo D., Aguiar, Marcos J. Burle de, Fernandes, Cassandro, Martelli Júnior, Hercílio

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  2. 2
    Identification of novel mutations in SHH and ZIC2 in a South American (ECLAMC) population with holoprosencephaly

    Identification of novel mutations in SHH and ZIC2 in a South American (ECLAMC) population with holoprosencephaly by Orioli, I M, Castilla, E E, Ming, J E, Nazer, J, Burle de Aguiar, M J, Llerena, J C, Muenke, M

    Published in Human genetics
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  3. 3
    Oral findings in Williams-Beuren syndrome

    Oral findings in Williams-Beuren syndrome by Ferreira, S-B-P, Viana, M-M, Maia, N-G-F, Leao, L-L, Machado, R-A, Coletta, R-D, de Aguiar, M-J-B, Martelli-Junior, H

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    Pfeiffer syndrome: clinical and genetic findings in five Brazilian families

    Pfeiffer syndrome: clinical and genetic findings in five Brazilian families by Júnior, Hercílio-Martelli, de Aquino, Sibele-Nascimento, Machado, Renato-Assis, Leão, Letícia-Lima, Coletta, Ricardo-Della, Burle-Aguiar, Marcos-José

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    Frequencies of phenylalanine hydroxylase mutations I65T, R252W, R261Q, R261X, IVS10nt11, V388M, R408W, Y414C, and IVS12nt1 in Minas Gerais, Brazil

    Frequencies of phenylalanine hydroxylase mutations I65T, R252W, R261Q, R261X, IVS10nt11, V388M, R408W, Y414C, and IVS12nt1 in Minas Gerais, Brazil by Santos, Luciana Lara dos, Magalhães, Myrian de Castro, Reis, Adriana de Oliveira, Starling, Ana Lúcia Pimenta, Januário, José Nélio, Fonseca, Cleusa Graça da, Aguiar, Marcos José Burle de, Carvalho, Maria Raquel Santos

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