Résultat(s) 1 - 5 résultats de 5 pour la requête 'Li, Mei-rong', Temps de recherche: 1,64s Affiner les résultats
  1. 1
    Correlation between MECP2 genotype and phenotype in Chinese patients with Rett syndrome
    Article

  2. 2
    Analysis of the parental origin of de novo MECP2 mutations and X chromosome inactivation in fifteen sporadic cases with Rett syndrome
    Autres auteurs: “...Li, Mei-rong...”
    Article

  3. 3
    Application of long range polymerase chain reaction and DNA direct sequencing in diagnosis of Rett syndrome
    Article

  4. 4
    X chromosome inactivation patterns in patients with Rett syndrome and their mothers and the parental origin of the priority inactive X chromosome
    Autres auteurs: “...Li, Mei-rong...”
    Article

  5. 5
    MECP2 gene mutations in twenty-six cases with atypical Rett syndrome
    Article

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