British journal of haematology, 2012-09, Vol.158 (6), p.805-809
- Martino, Alessandro
- Campa, Daniele
- Jamroziak, Krzysztof
- Reis, Rui Manuel
- Sainz, Juan
- Buda, Gabriele
- García-Sanz, Ramón
- Lesueur, Fabienne
- Marques, Herlander
- Moreno, Victor
- Jurado, Manuel
- Ríos, Rafael
- Szemraj-Rogucka, Zofia
- Szemraj, Janusz
- Tjønneland, Anne
- Overvad, Kim
- Vangsted, Annette Juul
- Vogel, Ulla
- Mikala, Gabor
- Kádár, Katalin
- Szombath, Gergely
- Varkonyi, Judit
- Orciuolo, Enrico
- Dumontet, Charles
- Gemignani, Federica
- Rossi, Anna Maria
- Landi, Stefano
- Petrini, Mario
- Houlston, Richard S.
- Hemminki, Kari
- Canzian, Federico
2012
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- Autor(en) / Beteiligte
- Martino, Alessandro
- Campa, Daniele
- Jamroziak, Krzysztof
- Reis, Rui Manuel
- Sainz, Juan
- Buda, Gabriele
- García-Sanz, Ramón
- Lesueur, Fabienne
- Marques, Herlander
- Moreno, Victor
- Jurado, Manuel
- Ríos, Rafael
- Szemraj-Rogucka, Zofia
- Szemraj, Janusz
- Tjønneland, Anne
- Overvad, Kim
- Vangsted, Annette Juul
- Vogel, Ulla
- Mikala, Gabor
- Kádár, Katalin
- Szombath, Gergely
- Varkonyi, Judit
- Orciuolo, Enrico
- Dumontet, Charles
- Gemignani, Federica
- Rossi, Anna Maria
- Landi, Stefano
- Petrini, Mario
- Houlston, Richard S.
- Hemminki, Kari
- Canzian, Federico
- Titel
- Impact of polymorphic variation at 7p15.3, 3p22.1 and 2p23.3 loci on risk of multiple myeloma
- Ist Teil von
- British journal of haematology, 2012-09, Vol.158 (6), p.805-809
- Ort / Verlag
- England: Blackwell Publishing Ltd
- Erscheinungsjahr
- 2012
- Quelle
- Wiley Online Library Journals Frontfile Complete
- Sprache
- Englisch
- Identifikatoren
- ISSN: 0007-1048eISSN: 1365-2141DOI: 10.1111/j.1365-2141.2012.09244.xTitel-ID: cdi_swepub_primary_oai_lup_lub_lu_se_5f32eb62_3997_411f_b517_193907d3b996
- Format
- –
- Schlagworte
- association study, Biological Specimen Banks, Chromosome Mapping, Chromosomes, Human, Pair 2 - genetics, Chromosomes, Human, Pair 2 - ultrastructure, Chromosomes, Human, Pair 3 - genetics, Chromosomes, Human, Pair 3 - ultrastructure, Chromosomes, Human, Pair 7 - genetics, Chromosomes, Human, Pair 7 - ultrastructure, Clinical Medicine, Female, Genes, myc, Genetic Predisposition to Disease, genetic susceptibilty, Genome-Wide Association Study, Genotype, Germany - epidemiology, Hematologi, Hematology, Humans, Klinisk medicin, Male, Medical and Health Sciences, Medicin och hälsovetenskap, multiple myeloma, Multiple Myeloma - epidemiology, Multiple Myeloma - genetics, Polymorphism, Single Nucleotide, Risk, single nucleotide polymorphism, United Kingdom - epidemiology