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Résultat(s) 1 - 8 résultats de 8 pour la requête '"EC 1.14.14.16"', Temps de recherche: 3,22s Affiner les résultats
  1. 1
    Analysis of clinical phenotype and genotype of Chinese children with disorders of sex development
    Sujets: “...NLM EC 1.14.14.16...”

    Article en ligne

  2. 2
    Analysis of phenotypes and genotypes in 66 patients with 21-hydroxylase deficiency identified by neonatal screening
    Sujets: “...NLM EC 1.14.14.16...”

    Article en ligne

  3. 3
    Determination of serum steroids in monitoring therapy of congenital adrenal hyperplasia
    Sujets: “...NLM EC 1.14.14.16...”
    Article

  4. 4
    Measuring adrenal autoantibody response interlaboratory concordance in the first international serum exchange for the determination of 21-hydroxylase autoantibodies
    Sujets: “...NLM EC 1.14.14.16...”

    Article en ligne

  5. 5
    Familial C4B deficiency and immune complex glomerulonephritis
    par Soto, K
    Publié dans: Clinical immunology (Orlando, Fla.) (2010)
    Sujets: “...NLM EC 1.14.14.16...”

    Article en ligne

  6. 6
    A discussion on risk factors of final height in 21-hydroxylase deficiency patients
    Sujets: “...NLM EC 1.14.14.16...”
    Article

  7. 7
    CYP21 gene point mutations study in 21-hydroxylase deficiency patients
    Sujets: “...NLM EC 1.14.14.16...”
    Article

  8. 8
    A PCR strategy that differentiates two alleles for a single base insertion within a T repeat
    par Lungu, O
    Publié dans: BioTechniques (1993)
    Sujets: “...NLM EC 1.14.14.16...”
    Article

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