Suggestion de sujets dans votre recherche.
Résultat(s) 1 - 7 résultats de 7 pour la requête '', Temps de recherche: 3,57s Affiner les résultats
  1. 1
    Unusual phenotype in patients with a hypomorphic mutation in the DCLRE1C gene IgG hypergammaglobulinemia with IgA and IgE deficiency

    Article en ligne

  2. 2
    Severe combined immunodeficiency (SCID) presenting in childhood, with agammaglobulinemia, associated with novel compound heterozygous mutations in DCLRE1C

    Article en ligne

  3. 3
    DNA recombination defects in Kuwait Clinical, immunologic and genetic profile

    Article en ligne

  4. 4
    Successful newborn screening for SCID in the Navajo Nation

    Article en ligne

  5. 5
    The many faces of Artemis-deficient combined immunodeficiency - Two patients with DCLRE1C mutations and a systematic literature review of genotype-phenotype correlation

    Article en ligne

  6. 6
    Omenn's syndrome occurring in patients without mutations in recombination activating genes
    Article

  7. 7
    Expansion of clonotype-restricted HLA-identical maternal CD4+ T cells in a patient with severe combined immunodeficiency and a homozygous mutation in the Artemis gene
    Article

Outils de recherche: S'abonner aux flux RSS — Envoyer cette recherche par courriel