|
[1]
|
Amselem, S., Nunes, V., Vidaud, M. et al. (1988). Determination of the Spectrum of β b Thalassemia Genes in Spain by Dot-Blot Analysis of Amplified β Globin DNA. American Journal of Human Genetics, 43, 95-100.
|
|
|
[2]
|
Antonarakis, S., Kazazian Jr., H. H., & Orkin, S. H. (1985). DNA Polymorphisms and Molecular Pathology of the Human Globin Gene Clusters. Human Genetics, 69, 1-14.
http://dx.doi.org/10.1007/BF00295521
|
|
|
[3]
|
Arnaiz-Villena, A. et al. (1999). Iberia: Population Genetics, Anthropology and Linguistics. Human Biology, 71, 725-743.
|
|
|
[4]
|
Benito, A. (1996). β Thalassemia in South-Western Spain: High Frequency of βIVSI-1(G-A) Mutation. British Journal of Haematology, 92, 336-338.
|
|
|
[5]
|
Bennani, C., Bouhass, R., Perrin-Percontal, P. et al. (1994). Anthropological Approach to the Heterogeneity of β Talassemia Mutations in Northern Africa. Human Biology, 66, 369-382.
|
|
|
[6]
|
Bosch, E. et al. (2001). High Resolution Analysis of Human Y Chromosome Variation Shows a Sharp Discontinuity and Limited Gene Flow between Northwestern Africa and the Iberian Peninsula. American Journal of Human Genetics, 68, 1019-1029.
http://dx.doi.org/10.1086/319521
|
|
|
[7]
|
Bruce-Chwatt, L. J., & Zulueta, J. (1980). Erradicacao da malária em Portugal. Lisboa: S. E. Saude.
|
|
|
[8]
|
Cabeda, J. M., Correia, C., Estevinho, A. et al. (1999). Unexpected Pattern of β Globin Mutations in β-Thalassaemia Patients from Northern Portugal. British Journal of Haematology, 105, 68-74.
http://dx.doi.org/10.1111/j.1365-2141.1999.01295.x
|
|
|
[9]
|
Cao, A., Gossens, M., & Pirastu, M. (1989). β Thalassaemia Mutations in Mediterranean Populations. British Journal of Haematology, 71, 309-312.
http://dx.doi.org/10.1111/j.1365-2141.1989.tb04285.x
|
|
|
[10]
|
Chibani, J., Vidaud, M., Duquesnoy, P., Bergé-Lefranc, J. L., Pirastu, M., Ellouze, F. et al. (1988). The Peculiar Spectrum of β Thalassemia Genes in Tunisia. Human Genetics, 78, 190-192.
http://dx.doi.org/10.1007/BF00278196
|
|
|
[11]
|
Encyclopaedia Britannica (1969). Encyclopaedia Britannica: 200th Anniversary Edition (Vol. 21). Chicago, IL: William Benton Publisher.
|
|
|
[12]
|
Fabiao, C. (1992). O passado protohistórico e romano. In J. Matoso (dir.), História de Portugal (Vol. 5, pp. 79-167). Lisboa: Editora Circulo de Leitores.
|
|
|
[13]
|
Faustino, P., Osório-Almeida, L., Barbot, J., Espírito-Santo, D., Goncalves, J., Romao, L. et al. (1992). Novel Promoter and Splice Junction Defects Add to the Genetic, Clinical or Geographic Heterogeneity of β Thalassemia in the Portuguese Population. Human Genetics, 89, 573-576.
http://dx.doi.org/10.1007/BF00219188
|
|
|
[14]
|
Faustino, P., Pacheco, P., Loureiro, P., Nogueira, P. J., & Lavinha, J. (1999). The Geographic Pattern of β Thalassaemia Mutations in the Portuguese Population. British Journal of Haematology, 107, 903-904.
http://dx.doi.org/10.1046/j.1365-2141.1999.01821.x
|
|
|
[15]
|
Flint, J., Harding, R., Clegg, J. B., & Boyce, A. J. (1993). Why Are Some Genetic Diseases Common? Human Genetics, 91, 91-117.
http://dx.doi.org/10.1007/BF00222709
|
|
|
[16]
|
Goncalves, I., Ducrocq, R., Lavinha, J., Nogueira, P. J., Peres, M. J., Picanao, I. et al. (1998). Combined Effect of Two Different Polymorphic Sequences within the Globin Cluster on the Level of HBF. American Journal of Hematology, 57, 269-276.
http://dx.doi.org/10.1002/(SICI)1096-8652(199804)57:4<269::AID-AJH1>3.0.CO;2-S
|
|
|
[17]
|
Goncalves, I., Henriques, A., Raimundo, A. et al. (2002). Fetal Hemoglobin Elevation in Hb Lepore Heterozygotes and Its Correlation with β Globin Cluster Linked Determinants. American Journal of Hematology, 69, 95-102.
http://dx.doi.org/10.1002/ajh.10019
|
|
|
[18]
|
Inez, F. et al. (1993). Contribuicao do rastreio de portadores para a prevencao da β talassémia e da drepanocitose na populacao portuguesa: Um estudo multicentrico. Arquivos INSA, 19, 27-31.
|
|
|
[19]
|
Lemsaddek, W. (2005). Analise molecular dos genes de beta e gama globina na populacao portuguesa e marroquina. Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa (UNL). Ph.D. Thesis.
|
|
|
[20]
|
Lemsaddek, W., Picanao, I., Seuanes, F. et al. (2003). Spectrum of β Thalassemia Mutations and HbF Levels in the Heterozygous Moroccan Population. American Journal of Hematology, 73, 161-168.
http://dx.doi.org/10.1002/ajh.10358
|
|
|
[21]
|
Lemsaddek, W., Picanao, I., Seuanes, F. et al. (2004). The β Thalassemia Mutation/Haplotype Distribution in the Moroccan Population. Hemoglobin, 28, 25-37.
http://dx.doi.org/10.1081/HEM-120028884
|
|
|
[22]
|
Maca-Mayer, N., González, A. M., Pestano, J., Flores, C., Larruga, J. M., & Cabrera, V. M. (2003). Mitochondrial DNA Transit between West Asia and North Africa Inferred from U6 Phylogeography. BMC Genetics, 4, 15.
|
|
|
[23]
|
Martins, M. C., Olim, G., Melo, J. et al. (1993). Hereditary Anaemias in Portugal: Epidemiology, Public Health Significance and Control. Journal of Medical Genetics, 30, 235-239.
http://dx.doi.org/10.1136/jmg.30.3.235
|
|
|
[24]
|
Mata, D. R. (1993). Los fenícios de época arcaica—Siglos VIII/VII a.C. en la Bahia de Cadiz. Estado de la cuestion. In E. Orientais (Ed.), Os Fenícios no território Português (Vol. 4, pp. 23-72). Lisboa: UNL, Instituto Oriental.
|
|
|
[25]
|
Pirastu, M. et al. (1988). Delineation of Specific β Thalassemia Mutations in High Risk Areas of Italy: A Prerequisite for Prenatal Diagnosis. Blood, 71, 983-988.
|
|
|
[26]
|
Ribeiro, M. L. et al. (1997). Genetic Heterogeneity of β Thalassemia in Populations of the Iberian Peninsula. Hemoglobin, 21, 261-269.
http://dx.doi.org/10.3109/03630269708997387
|
|
|
[27]
|
Rosatelli, M. C., Tuveri, T., Scalas, M. T., Leoni, G. B., Sardu, R., Faà, V. et al. (1992). Molecular Screening and Fetal Diagnosis of β Thalassemia in the Italian Population. Human Genetics, 89, 585-589.
|
|
|
[28]
|
Rouabhi, F., Amselem, S., Krishnamoorthy, R., Adjrad, L., Girot, R., Chardin, P. et al. (1988). DNA Haplotype Distribution in Algerian β Thalassaemia Patients. Human Genetics, 79, 373-376.
http://dx.doi.org/10.1007/BF00282180
|
|
|
[29]
|
Schiliro, G., di Gregorio, F., Samperi, P., Mirabile, E., Liang, R., Cürük, M. A. et al. (1995). Genetic Heterogeneity of β Thalassemia in Southeast Sicily. American Journal of Hematology, 48, 5-11.
http://dx.doi.org/10.1002/ajh.2830480103
|
|
|
[30]
|
Sforza, C. et al. (1993). Demic Expansions and Human Evolution. Science, 259, 639-646.
http://dx.doi.org/10.1126/science.8430313
|
|
|
[31]
|
Tavares, A. A. (1993). Fenícios e Massienos na Península Ibérica. In E. Orientais (Ed.), Os Fenícios no território Português (Vol. 4). Lisboa: Instituto Oriental, UNL.
|
|
|
[32]
|
Torres, C. (1992). O Gharb Al Andaluz. In J. Matoso (dir.), História de Portugal (Vol. 5, pp. 363-441). Lisboa: Circulo de Leitores.
|
|
|
[33]
|
Varela Gomes, M. (1993). O estabelecimento fenício-púnico do Cerro da Rocha Branca (Silves). In E. Orientais (Ed.), Os Fenícios no território (Vol. 4, pp. 73-107). Lisboa: Instituto Oriental, UNL.
|
|
|
[34]
|
Waye, J. S., Borys, S., Eng, B., Patterson, M., Chui, D. H. K., Badr El-Din, O. M. K. et al. (1999). Spectrum of β Thalassemia Mutations in Egypt. Hemoglobin, 23, 225-261.
http://dx.doi.org/10.3109/03630269909005706
|
|