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  1. 1
    DNA recombination defects in Kuwait Clinical, immunologic and genetic profile

    Article en ligne

  2. 2
    Mutations in Recombination Activating Gene 1 and 2 in patients with severe combined immunodeficiency disorders in Egypt

    Article en ligne

  3. 3
    Clinical phenotype and gene diagnostic analysis of Omenn syndrome
    Article

  4. 4
    Analysis of mutations and recombination activity in RAG-deficient patients

    Article en ligne

  5. 5
    Novel mutations in RAG1/2 and ADA genes in Israeli patients presenting with T-B-SCID or Omenn syndrome

    Article en ligne

  6. 6
    More than just SCID--the phenotypic range of combined immunodeficiencies associated with mutations in the recombinase activating genes (RAG) 1 and 2

    Article en ligne

  7. 7
    GvHD-associated cytokine polymorphisms do not associate with Omenn syndrome rather than T-B- SCID in patients with defects in RAG genes
    Article

  8. 8
    Omenn's syndrome occurring in patients without mutations in recombination activating genes
    Article

  9. 9
    Evolution of a T-B- SCID into an Omenn syndrome phenotype following parainfluenza 3 virus infection
    Article

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