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Results: 1-25 | 26-28 |
Results: 26-28/28
A novel splice site mutation in a Brazilian patient with hereditary antithrombin deficiency type I
Authors: Arnaldi, LAT Polimeno, NC Arruda, VR Annichino-Bizzacchi, JM
Citation: Lat. Arnaldi et al., A novel splice site mutation in a Brazilian patient with hereditary antithrombin deficiency type I, HUMAN HERED, 49(2), 1999, pp. 119-120
A novel nonsense mutation 6,E-X in the protein S gene causes type I deficiency
Authors: Pugliese, L Arruda, VR Annichino-Bizzacchi, JM
Citation: L. Pugliese et al., A novel nonsense mutation 6,E-X in the protein S gene causes type I deficiency, HUMAN HERED, 49(2), 1999, pp. 121-122
Determination of the allele frequencies of three polymorphisms in the promoter region of the human protein C gene in three Brazilian ethnic groups
Authors: Mendes, CPO Hackel, C Arruda, VR Annichino-Bizzacchi, JM
Citation: Cpo. Mendes et al., Determination of the allele frequencies of three polymorphisms in the promoter region of the human protein C gene in three Brazilian ethnic groups, HUMAN HERED, 49(1), 1999, pp. 27-30
Risultati: 1-25 | 26-28 |