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Results: 1-5 |
Results: 5

Authors: Gjetting, T Romstad, A Haavik, J Knappskog, PM Acosta, AX Silva, WA Zago, MA Guldberg, P Guttler, F
Citation: T. Gjetting et al., A phenylalanine hydroxylase amino acid polymorphism with implications for molecular diagnostics, MOL GEN MET, 73(3), 2001, pp. 280-284

Authors: Acosta, AX Silva, WA Carvalho, TM Gomes, M Zago, MA
Citation: Ax. Acosta et al., Mutations of the phenylalanine hydroxylase (PAH) gene in Brazilian patients with phenylketonuria, HUM MUTAT, 17(2), 2001, pp. 122-130

Authors: Acosta, AX Peres, LC Chimelli, LC Pina-Neto, JM
Citation: Ax. Acosta et al., Raine dysplasia: a Brazilian case with a mild radiological involvement, CLIN DYSMOR, 9(2), 2000, pp. 99-101

Authors: Melo, DC Pina-Neto, JM Acosta, AX Daniel, J de Castro, V Santos, AC
Citation: Dc. Melo et al., Neuroimaging and echocardiographic findings in Sotos syndrome, AM J MED G, 90(5), 2000, pp. 432-433

Authors: Melo, DG Acosta, AX de Pina-Neto, JM
Citation: Dg. Melo et al., Syndrome of psychomotor retardation, bulbous nose, and epilepsy (Hernandezsyndrome): A Brazilian case, CLIN DYSMOR, 8(4), 1999, pp. 301-303
Risultati: 1-5 |