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De novo mosaic MECP2 mutation in a female with Rett syndrome.
Alexandrou, Angelos; Papaevripidou, Ioannis; Alexandrou, Ioanna Maria; Theodosiou, Athina; Evangelidou, Paola; Kousoulidou, Ludmila; Tanteles, George; Christophidou-Anastasiadou, Violetta; Sismani, Carolina.
Afiliação
  • Alexandrou A; Department of Cytogenetics and Genomics The Cyprus Institute of Neurology and Genetics Nicosia Cyprus.
  • Papaevripidou I; Department of Cytogenetics and Genomics The Cyprus Institute of Neurology and Genetics Nicosia Cyprus.
  • Alexandrou IM; Department of Cytogenetics and Genomics The Cyprus Institute of Neurology and Genetics Nicosia Cyprus.
  • Theodosiou A; Department of Cytogenetics and Genomics The Cyprus Institute of Neurology and Genetics Nicosia Cyprus.
  • Evangelidou P; Department of Cytogenetics and Genomics The Cyprus Institute of Neurology and Genetics Nicosia Cyprus.
  • Kousoulidou L; Department of Cytogenetics and Genomics The Cyprus Institute of Neurology and Genetics Nicosia Cyprus.
  • Tanteles G; Department of Clinical Genetics The Cyprus Institute of Neurology and Genetics Nicosia Cyprus.
  • Christophidou-Anastasiadou V; Department of Clinical Genetics The Cyprus Institute of Neurology and Genetics Nicosia Cyprus.
  • Sismani C; Archbishop Makarios III Medical Centre Nicosia Cyprus.
Clin Case Rep ; 7(2): 366-370, 2019 Feb.
Article em En | MEDLINE | ID: mdl-30847208

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2019 Tipo de documento: Article