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Filtros: Autor es Marques, H  [Restablecer todos los filtros]
A B C D E F G H I J K L M N O P Q R S T U V W X Y Z 
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Campa D, Martino A, Sainz J, Buda G, Jamroziak K, Weinhold N, et al. Comprehensive investigation of genetic variation in the 8q24 region and multiple myeloma risk in the IMMEnSE consortium. British journal of haematology. 2012;157(3):331-8. Abstract
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Martino A, Sainz J, Buda G, Jamroziak K, Reis RM, García-Sanz R, et al. Genetics and molecular epidemiology of multiple myeloma: the rationale for the IMMEnSE consortium (review). International journal of oncology. 2012;40(3):625-38. Abstract
I
Martino A, Campa D, Jamroziak K, Reis RM, Sainz J, Buda G, et al. Impact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myeloma. British journal of haematology. 2012;158(6):805-9.
P
Martino A, Sainz J, Manuel Reis R, Moreno V, Buda G, Lesueur F, et al. Polymorphisms in regulators of xenobiotic transport and metabolism genes PXR and CAR do not affect multiple myeloma risk: a case-control study in the context of the IMMEnSE consortium. Journal of human genetics. 2013;58(3):155-9. Abstract