Treffer 1 - 5 von 5 für Suche 'Li, Mei-rong', Suchdauer: 1,94s Treffer weiter einschränken
  1. 1
    Analysis of the parental origin of de novo MECP2 mutations and X chromosome inactivation in fifteen sporadic cases with Rett syndrome
    Weitere Verfasser: “...Li, Mei-rong...”
    Aufsatz

  2. 2
    Correlation between MECP2 genotype and phenotype in Chinese patients with Rett syndrome
    Aufsatz

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

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

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

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