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pro vyhledávání: '"Salle, B. de la"'
Autor:
Traeger-Synodinos, J., Harteveld, C.L., Old, J.M., Petrou, M., Galanello, R., Giordano, P., Angastioniotis, M., Salle, B. de la, Henderson, S., May, A., EMQN Haemoglobinopathies Best
Publikováno v:
European Journal of Human Genetics
European Journal of Human Genetics, 23(4), 426-437
European Journal of Human Genetics, 23(4), 426-437
Haemoglobinopathies constitute the commonest recessive monogenic disorders worldwide, and the treatment of affected individuals presents a substantial global disease burden. Carrier identification and prenatal diagnosis represent valuable procedures
Autor:
Wilkinson, F. L., Bigger, B. W., Eke, Z., Brereton, M., Salle, B. de la, Overfield, J., Hyde, K.
Publikováno v:
British Journal of Biomedical Science; January 2009, Vol. 66 Issue: 4 p223-224, 2p