Search Results - Boavida, M.G.

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  1. 1
    Influence of hOGG1 genotype on the frequencies of stable and unstable chromosome aberrations in radiation-exposed individuals

    Influence of hOGG1 genotype on the frequencies of stable and unstable chromosome aberrations in radiation-exposed individuals by Gil, F, Louro, H, Dias, A, Monteiro-Gil, O, Painço, P, Teixeira, T, Sousa, C, Costa, P, Boavida, M.G, Silva, M.J

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  2. 2
    Novel MLH1 mutations and a novel MSH2 polymorphism identified by SSCP and DHPLC in Portuguese HNPCC families

    Novel MLH1 mutations and a novel MSH2 polymorphism identified by SSCP and DHPLC in Portuguese HNPCC families by Isidro, G., Matos, S., Gonçalves, V., Cavaleiro, C., Antunes, O., Marinho, C., Soares, J., Boavida, M.G.

    Published in Human mutation
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  3. 3
    Novel MLH1 mutations and a novel MSH2 polymorphism identified by SSCP and DHPLC in Portuguese HNPCC families: MUTATIONS IN BRIEF

    Novel MLH1 mutations and a novel MSH2 polymorphism identified by SSCP and DHPLC in Portuguese HNPCC families: MUTATIONS IN BRIEF by Isidro, G., Matos, S., Gonçalves, V., Cavaleiro, C., Antunes, O., Marinho, C., Soares, J., Boavida, M.G.

    Published in Human mutation
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  4. 4
    Low frequency noise and whole-body vibration cause increased levels of sister chromatid exchange in splenocytes of exposed mice

    Low frequency noise and whole-body vibration cause increased levels of sister chromatid exchange in splenocytes of exposed mice by Silva, M.J., Dias, A., Barreta, A., Nogueira, P.J., Castelo-Branco, N.A.A., Boavida, M.G.

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  5. 5
    Four novel MSH2 / MLH1 gene mutations in Portuguese HNPCC families

    Four novel MSH2 / MLH1 gene mutations in Portuguese HNPCC families by Isidro, G., Veiga, I., Matos, P., Almeida, S., Bizarro, S., Marshall, B., Baptista, M., Leite, J., Regateiro, F., Soares, J., Castedo, S., Boavida, M.G.

    Published in Human mutation
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  6. 6
    Translocation (8;17;15;21)(q22;q23;q15;q22) in acute myeloid leukemia (M2)

    Translocation (8;17;15;21)(q22;q23;q15;q22) in acute myeloid leukemia (M2) by Vieira, Luı́s, Oliveira, Vanessa, Ambrósio, Ana P., Marques, Bárbara, Pereira, Ana M., Hagemeijer, Anne, Boavida, M.G.

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  7. 7
    Eleven novel APC mutations identified in Portuguese FAP families

    Eleven novel APC mutations identified in Portuguese FAP families by Isidro, G., Matos, P., Almeida, S., Claudino, S., Marshall, B., Soares, J., Leite, J., Regateiro, F., Brito, M.J., Giria, J., Castro, C., Ramos, J., Novais, L., Morna, H., Medeira, A., Castedo, S., Boavida, M.G.

    Published in Human mutation
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  8. 8
    Translocation (8;17;15;21)(q22;q23;q15;q22) in acute myeloid leukemia (M2): a four-way variant of t(8;21)

    Translocation (8;17;15;21)(q22;q23;q15;q22) in acute myeloid leukemia (M2): a four-way variant of t(8;21) by Vieira, Luı́s, Oliveira, Vanessa, Ambrósio, Ana P., Marques, Bárbara, Pereira, Ana M., Hagemeijer, Anne, Boavida, M.G.

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  9. 9
    Molecular cytogenetic characterization of rearrangements involving 12p in leukemia

    Molecular cytogenetic characterization of rearrangements involving 12p in leukemia by Vieira, L., Marques, B., Cavaleiro, C., Ambrósio, A.P., Jorge, M., Neto, A., Costa, J.M., Júnior, E.C., Boavida, M.G.

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  10. 10
    Isochromosome 14q in refractory anemia

    Isochromosome 14q in refractory anemia by Boavida, M.G., Ambrósio, P., Dhermy, D., Silva, C., Correia, M.E.

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  11. 11
    Sister chromatid exchange analysis in workers exposed to noise and vibration

    Sister chromatid exchange analysis in workers exposed to noise and vibration by Silva, M.J., Carothers, A., Castelo Branco, N., Dias, A., Boavida, M.G.

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  12. 12
    Detection and identification of mutations in the APC gene in portuguese fap families using the protein truncation test and SSCP

    Detection and identification of mutations in the APC gene in portuguese fap families using the protein truncation test and SSCP by Marshall, B., Isidro, G., Carvalhas, R., Veiga, I., Ramos, J.S., Viana, L., Santos, G., Castedo, S., Boavida, M.G.

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